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A Complex Intervention for Chronically Fatigued Lymphoma Survivors

Primary Purpose

Chronic Fatigue Syndrome

Status
Recruiting
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Interdisciplinary complex intervention
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Fatigue Syndrome focused on measuring lymphoma, cancer survivorship, physical activity, nutrition, patient education, cognitive behavioral program

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Survivors of Hodgkin and aggressive non-Hodgkin lymphoma
  • Not indolent non-Hodgkin lymphoma
  • Not CNS lymphoma at diagnosis
  • Not second cancer
  • Not ongoing cancer treatment
  • Chronic fatigue measured by Chalder Fatigue Questionnaire
  • Diagnosed 2010-2020
  • Received treatment with curative intent
  • 18 - 70 years old at inclusion
  • > 2 years since last treatment
  • Able to understand the Norwegian language
  • Participation approval from oncologist in the project group

Exclusion Criteria:

  • Persisting fatigue > 1 year before the cancer diagnosis
  • Somatic/physical conditions (i.e. severe heart failure/disease, lung disease, use of wheelchair /crutches)
  • Psychiatric or mental disorders (i.e. dementia, severe depression, schizophrenia)
  • Use of stimulants for ADHD
  • Substance abuse disorder

Sites / Locations

  • Oslo University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Interdisciplinary complex intervention

Usual care

Arm Description

Six months after the intervention period (T3), the participants randomized to usual care will be offered a modified version of the intervention in line with their personally expressed needs.

Outcomes

Primary Outcome Measures

Changes of the level of fatigue (physical-, mental- and total fatigue) assessed by the Chalder Fatigue Questionnaire
The Fatigue Questionnaire consists of 11 questions, distributed on a physical fatigue scale (7 items) and mental fatigue scale (4 items) Each item is scored from 0 to 3. This provides a physical fatigue score from 0 to 21, mental fatigue score from 0 to 12, and total score from 0 to 33. Higher score implies more fatigue.

Secondary Outcome Measures

Change of the level of fatigue assessed by Chalder Fatigue Questionnaire
The Fatigue Questionnaire consists of 11 questions, distributed on a physical fatigue scale (7 items) and mental fatigue scale (4 items) Each item is scored from 0 to 3, providing a total score from 0 to 33. Higher score implies more fatigue.
Change of the level of fatigue assessed by Chalder Fatigue Questionnaire
The Fatigue Questionnaire consists of 11 questions, distributed on a physical fatigue scale (7 items) and mental fatigue scale (4 items) Each item is scored from 0 to 3, providing a total score from 0 to 33. Higher score implies more fatigue.
Change in daily functioning assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
The questionnaire includes five functioning scales (physical, role, cognitive, emotional and social).All of the scales range in score from 0 to 100. A high score for a functional scale represents a high / healthy level of functioning.
Change in daily functioning assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
The questionnaire includes five functioning scales (physical, role, cognitive, emotional and social).All of the scales range in score from 0 to 100. A high score for a functional scale represents a high / healthy level of functioning.
Change in daily functioning assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
The questionnaire includes five functioning scales (physical, role, cognitive, emotional and social).All of the scales range in score from 0 to 100. A high score for a functional scale represents a high / healthy level of functioning.
Change in global quality of life assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Change in global quality of life assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Change in global quality of life assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Change in work ability assessed by the Work Ability Index scale
Current work ability is rated compared with the lifetime best on a scale from 0 to 10. Higher score implies higher work ability.
Change in work ability assessed by the Work Ability Index scale
Current work ability is rated compared with the lifetime best on a scale from 0 to 10. Higher score implies higher work ability.
Change in work ability assessed by the Work Ability Index scale
Current work ability is rated compared with the lifetime best on a scale from 0 to 10. Higher score implies higher work ability.
Change in work ability assessed by the Work Ability Index: physical demands of the job
Assessed by rating work ability in relation to the physical demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Change in work ability assessed by the Work Ability Index: physical demands of the job
Assessed by rating work ability in relation to the physical demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Changes in work ability assessed by the Work Ability Index: physical demands of the job
Assessed by rating work ability in relation to the physical demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Changes in work ability assessed by the Work Ability Index: psychological demands of the job
Assessed by rating work ability in relation to the psychological demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Change in work ability assessed by the Work Ability Index: psychological demands of the job
Assessed by rating work ability in relation to the psychological demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Change in work ability assessed by the Work Ability Index: psychological demands of the job
Assessed by rating work ability in relation to the psychological demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Change in cardiorespiratory fitness assessed by cardio-pulmonary exercise testing (CPET)
Peak oxygen uptake (VO2peak) is measured
Change in cardiorespiratory fitness assessed by cardio-pulmonary exercise testing (CPET)
Peak oxygen uptake (VO2peak) is measured
Change in cardiorespiratory fitness assessed by cardio-pulmonary exercise testing (CPET)
Peak oxygen uptake (VO2peak) is measured
Change in cardiorespiratory fitness assessed by a treadmill test
In cases where participants do not have the opportunity to travel for physical fitness tests, cardiorespiratory fitness will be assessed by an indirect treadmill test (modified Balke protocol) at their local physiotherapist. Time to exhaustion will be used as an indicator of cardiorespiratory fitness.
Change in cardiorespiratory fitness assessed by a treadmill test
In cases where participants do not have the opportunity to travel for physical fitness tests, cardiorespiratory fitness will be assessed by an indirect treadmill test (modified Balke protocol) at their local physiotherapist. Time to exhaustion will be used as an indicator of cardiorespiratory fitness.
Change in cardiorespiratory fitness assessed by a treadmill test
In cases where participants do not have the opportunity to travel for physical fitness tests, cardiorespiratory fitness will be assessed by an indirect treadmill test (modified Balke protocol) at their local physiotherapist. Time to exhaustion will be used as an indicator of cardiorespiratory fitness.
Change in lower body muscle strength assessed by leg press
The one-repetition maximum (1RM) test (the maximal workload that can be lifted once)) in leg press.
Change in lower body muscle strength assessed by leg press
The one-repetition maximum (1RM) test (the maximal workload that can be lifted once)) in leg press.
Change in lower body muscle strength assessed by leg press
The one-repetition maximum (1RM) test (the maximal workload that can be lifted once)) in leg press.
Change in upper body muscle strength assessed by push-ups
The maximum number of push-ups that can be performed in one set
Change in upper body muscle strength assessed by push-ups
The maximum number of push-ups that can be performed in one set
Change in upper body muscle strength assessed by push-ups
The maximum number of push-ups that can be performed in one set
Change in level of depressive symptoms assessed by the Patient Health Questionnaire-9
Each of the 9 items is scored from 0-3, providing a total score from 0 to 27. A higher score implies higher level of depressive symptoms.
Change in level of depressive symptoms assessed by the Patient Health Questionnaire-9
Each of the 9 items is scored from 0-3, providing a total score from 0 to 27. A higher score implies higher level of depressive symptoms.
Change in level of depressive symptoms assessed by the Patient Health Questionnaire-9
Each of the 9 items is scored from 0-3, providing a total score from 0 to 27. A higher score implies higher level of depressive symptoms.
Change in level of anxiety symptoms assessed by the General Anxiety Disorder 7-items (GAD7).
Each of the 7 items is scored from 0-3, providing a total score from 0-21. A higher score implies higher level of anxiety symptoms.
Change in level of anxiety symptoms assessed by the General Anxiety Disorder 7-items (GAD7).
Each item is scored from 0-3, providing a total score from 0-21. A higher score implies higher level of anxiety symptoms.
Change in level of anxiety symptoms assessed by the General Anxiety Disorder 7-items (GAD7).
Each of the 7 items is scored from 0-3, providing a total score from 0-21. A higher score implies higher level of anxiety symptoms.
Changes in sense of exercise competence assessed by the Perceived Competence Scale.
The scale consists of 4 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 0 to 7 is calculated based on the mean score of the items, with increasing score implying higher exercise competence.
Change in sense of exercise competence assessed by the Perceived Competence Scale.
The scale consists of 4 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 0 to 7 is calculated based on the mean score of the items, with increasing score implying higher exercise competence.
Change in sense of exercise competence assessed by the Perceived Competence Scale.
The scale consists of 4 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 0 to 7 is calculated based on the mean score of the items, with increasing score implying higher exercise competence.
Change in satisfaction with life assessed by the Satisfaction With Life Scale.
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher satisfaction with life.
Changes in satisfaction with life assessed by the Satisfaction With Life Scale.
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher satisfaction with life.
Change in satisfaction with life assessed by the Satisfaction With Life Scale.
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher satisfaction with life.
Change in sense of vitality assessed by the Subjective Vitality Scale
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher sense of vitality.
Change in sense of vitality assessed by the Subjective Vitality Scale
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher sense of vitality.
Changes in sense of vitality assessed by the Subjective Vitality Scale
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher sense of vitality.
Change in adherence to the Norwegian food-based dietary guidelines assessed by DIGIKOST-FFQ
DIGIKOST-FFQ is a food frequency questionnaire aiming to benchmark against the Norwegian food-based dietary guidelines.
Changes in adherence to the Norwegian food-based dietary guidelines assessed by DIGIKOST-FFQ
DIGIKOST-FFQ is a food frequency questionnaire aiming to benchmark against the Norwegian food-based dietary guidelines.
Change in adherence to the Norwegian food-based dietary guidelines assessed by DIGIKOST-FFQ
DIGIKOST-FFQ is a food frequency questionnaire aiming to benchmark against the Norwegian food-based dietary guidelines.
Change in general health measured by European Quality of Life Five-Dimension Scale Questionnaire (EQ-5D)
EQ-5D consists of five dimensions (mobility, self-care, usual activities, pain & discomfort, anxiety & depression), each of which has five severity levels that are described by statements appropriate to that dimension.
Change in general health measured by European Quality of Life Five-Dimension Scale Questionnaire (EQ-5D)
EQ-5D consists of five dimensions (mobility, self-care, usual activities, pain & discomfort, anxiety & depression), each of which has five severity levels that are described by statements appropriate to that dimension.
Change in general health measured by European Quality of Life Five-Dimension Scale Questionnaire (EQ-5D)
EQ-5D consists of five dimensions (mobility, self-care, usual activities, pain & discomfort, anxiety & depression), each of which has five severity levels that are described by statements appropriate to that dimension.
Change in quality of life among the relatives measured by Research and Development 36-term Short Form Health Survey (RAND SF-36)
RAND-36 comprises 36 items that assess eight health concepts: physical functioning, role limitations caused by physical health problems, role limitations caused by emotional problems, social functioning, emotional well-being, energy/fatigue, pain, and general health perceptions. Physical and mental health summary scores are also derived from the eight RAND-36 scales.All questions are scored on a scale from 0 to 100, with 100 representing the highest level of functioning possible.
Change in quality of life among the relatives measured by Research and Development 36-term Short Form Health Survey (RAND SF-36)
RAND-36 comprises 36 items that assess eight health concepts: physical functioning, role limitations caused by physical health problems, role limitations caused by emotional problems, social functioning, emotional well-being, energy/fatigue, pain, and general health perceptions. Physical and mental health summary scores are also derived from the eight RAND-36 scales.All questions are scored on a scale from 0 to 100, with 100 representing the highest level of functioning possible.
Change in quality of life among the relatives measured by Research and Development 36-term Short Form Health Survey (RAND SF-36)
RAND-36 comprises 36 items that assess eight health concepts: physical functioning, role limitations caused by physical health problems, role limitations caused by emotional problems, social functioning, emotional well-being, energy/fatigue, pain, and general health perceptions. Physical and mental health summary scores are also derived from the eight RAND-36 scales.All questions are scored on a scale from 0 to 100, with 100 representing the highest level of functioning possible.
Change in quality of life among the relatives measured by the global health status / QoL scale from the European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Change in quality of life among the relatives measured by the global health status / QoL scale from the European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Change in quality of life among the relatives measured by the global health status / QoL scale from the European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Cost-effectiveness calculated based on measurements of health-related QoL and resource use (costs related to the intervention.
Combining information about health-related QoL will give quality-adjusted life-years, while valuation of resource use using standard principles of health economic evaluation will provide estimates of costs

Full Information

First Posted
November 10, 2021
Last Updated
October 3, 2022
Sponsor
Oslo University Hospital
Collaborators
University of Oslo, Norwegian School of Sport Sciences, UiT The Arctic University of Norway, Norwegian University of Science and Technology, Diakonhjemmet Hospital, University of Alberta, St. Olavs Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05130099
Brief Title
A Complex Intervention for Chronically Fatigued Lymphoma Survivors
Official Title
A Complex Intervention for a Complex Symptom - a Randomized Controlled Trial in Chronically Fatigued Lymphoma Survivors
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 20, 2021 (Actual)
Primary Completion Date
April 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
Collaborators
University of Oslo, Norwegian School of Sport Sciences, UiT The Arctic University of Norway, Norwegian University of Science and Technology, Diakonhjemmet Hospital, University of Alberta, St. Olavs Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The present study is a randomized controlled trial (RCT) with an overall objective to examine the effect of an interdisciplinary complex intervention on the level of fatigue in lymphoma survivors with chronic fatigue. Secondary aims are to examine the effects of the intervention on daily functioning, work ability, physical fitness, QoL and cortisol secretion among the survivors, on QoL of their relatives and on the societal costs.The intervention will last for 12+12 weeks and include four components; patient education, supervised physical exercise, cognitive behavioral program and nutritional counselling. Outcomes will be assessed at baseline,post-intervention (12 weeks after baseline) and at 3-month and 6-month follow-up after completed intervention.
Detailed Description
Chronic fatigue (CF) is a subjective experience of substantial lack of energy, exhaustion and cognitive difficulties lasting for six months or longer. CF is one of the most common and distressing late effects after cancer, affecting 15-35 % of survivors, often for years beyond treatment. Despite the high prevalence and the huge negative consequences of CF on daily functioning and QoL and the economic and societal costs, effective treatment of CF and standardized follow-up care are currently lacking. Today, there is no curative treatment of CF. However, several modifiable behavioral factors including emotional distress, physical inactivity, sleep disturbances and unhealthy diets are found to be associated with CF. So far, most of the interventions aiming to reduce fatigue during and shortly after cancer treatment have targeted only one of these factors at a time, with small to moderate effect sizes. No prior study has examined if CF in cancer survivors is better treated by a complex intervention targeting combinations of these factors, an approach which seems logical due to the complexity of the symptom. The project is a two-armed RCT in which chronically fatigued lymphoma survivors are randomized to an interdisciplinary complex intervention or to usual care. Eligible participants will receive written information about the study by mail. Survivors who perceive themselves as having physical and mental fatigue, and who are willing to participate, will be asked to fill out and return the Chalder Fatigue Questionnaire (FQ) to the study coordinator. Those who have chronic fatigue as measured by the FQ will be invited to a medical screening by an oncologist in the project group, for evaluation of inclusion. The interdisciplinary complex intervention will last for 12 + 12 weeks and include four components; patient education, physical exercise (and follow-up), cognitive behavioral program and nutritional counselling, organized in a systematic way, i.e. a standardized patient care pathway. All outcomes will be assessed in all participants at four points; pre-intervention (baseline) (T0), post-intervention (12 weeks after baseline) (T1) and at 3-month (T2) and 6-month (T3) after T1.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Fatigue Syndrome
Keywords
lymphoma, cancer survivorship, physical activity, nutrition, patient education, cognitive behavioral program

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
148 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Interdisciplinary complex intervention
Arm Type
Experimental
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Six months after the intervention period (T3), the participants randomized to usual care will be offered a modified version of the intervention in line with their personally expressed needs.
Intervention Type
Other
Intervention Name(s)
Interdisciplinary complex intervention
Intervention Description
The interdisciplinary complex intervention lasts 12 weeks and includes the 4 following components; Patient-education: a 2-hours group-based digital session, including information about fatigue, training theory, psychological strategies and nutrition, all in relation to chronic fatigue (CF). Physical exercise program: two weekly sessions with aerobic exercise and resistance training. The participants are instructed to do the same program in the unsupervised sessions as in the supervised sessions. After the first 12 weeks exercise period, the participant and the physiotherapist makes an individually tailored plan for exercise and follow-up the next 12 weeks. Cognitive behavioral program: 6 group-based online sessions lead by two psychologists, based on elements from cognitive behavioral therapy to reduce and/or manage CF. Each session lasts for 135 minutes. Nutritional counselling: 3 individual sessions by a clinical dietitian. Each session lasts for 30-60 minutes.
Primary Outcome Measure Information:
Title
Changes of the level of fatigue (physical-, mental- and total fatigue) assessed by the Chalder Fatigue Questionnaire
Description
The Fatigue Questionnaire consists of 11 questions, distributed on a physical fatigue scale (7 items) and mental fatigue scale (4 items) Each item is scored from 0 to 3. This provides a physical fatigue score from 0 to 21, mental fatigue score from 0 to 12, and total score from 0 to 33. Higher score implies more fatigue.
Time Frame
From baseline (T0) to 12 weeks (T1)
Secondary Outcome Measure Information:
Title
Change of the level of fatigue assessed by Chalder Fatigue Questionnaire
Description
The Fatigue Questionnaire consists of 11 questions, distributed on a physical fatigue scale (7 items) and mental fatigue scale (4 items) Each item is scored from 0 to 3, providing a total score from 0 to 33. Higher score implies more fatigue.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change of the level of fatigue assessed by Chalder Fatigue Questionnaire
Description
The Fatigue Questionnaire consists of 11 questions, distributed on a physical fatigue scale (7 items) and mental fatigue scale (4 items) Each item is scored from 0 to 3, providing a total score from 0 to 33. Higher score implies more fatigue.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in daily functioning assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
Description
The questionnaire includes five functioning scales (physical, role, cognitive, emotional and social).All of the scales range in score from 0 to 100. A high score for a functional scale represents a high / healthy level of functioning.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in daily functioning assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
Description
The questionnaire includes five functioning scales (physical, role, cognitive, emotional and social).All of the scales range in score from 0 to 100. A high score for a functional scale represents a high / healthy level of functioning.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in daily functioning assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
Description
The questionnaire includes five functioning scales (physical, role, cognitive, emotional and social).All of the scales range in score from 0 to 100. A high score for a functional scale represents a high / healthy level of functioning.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in global quality of life assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
Description
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in global quality of life assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
Description
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in global quality of life assessed by European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
Description
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in work ability assessed by the Work Ability Index scale
Description
Current work ability is rated compared with the lifetime best on a scale from 0 to 10. Higher score implies higher work ability.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in work ability assessed by the Work Ability Index scale
Description
Current work ability is rated compared with the lifetime best on a scale from 0 to 10. Higher score implies higher work ability.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in work ability assessed by the Work Ability Index scale
Description
Current work ability is rated compared with the lifetime best on a scale from 0 to 10. Higher score implies higher work ability.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in work ability assessed by the Work Ability Index: physical demands of the job
Description
Assessed by rating work ability in relation to the physical demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in work ability assessed by the Work Ability Index: physical demands of the job
Description
Assessed by rating work ability in relation to the physical demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Changes in work ability assessed by the Work Ability Index: physical demands of the job
Description
Assessed by rating work ability in relation to the physical demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Changes in work ability assessed by the Work Ability Index: psychological demands of the job
Description
Assessed by rating work ability in relation to the psychological demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in work ability assessed by the Work Ability Index: psychological demands of the job
Description
Assessed by rating work ability in relation to the psychological demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in work ability assessed by the Work Ability Index: psychological demands of the job
Description
Assessed by rating work ability in relation to the psychological demands of the job, by the following response alternatives: very good, rather good, moderate, rather poor or very poor
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in cardiorespiratory fitness assessed by cardio-pulmonary exercise testing (CPET)
Description
Peak oxygen uptake (VO2peak) is measured
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in cardiorespiratory fitness assessed by cardio-pulmonary exercise testing (CPET)
Description
Peak oxygen uptake (VO2peak) is measured
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in cardiorespiratory fitness assessed by cardio-pulmonary exercise testing (CPET)
Description
Peak oxygen uptake (VO2peak) is measured
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in cardiorespiratory fitness assessed by a treadmill test
Description
In cases where participants do not have the opportunity to travel for physical fitness tests, cardiorespiratory fitness will be assessed by an indirect treadmill test (modified Balke protocol) at their local physiotherapist. Time to exhaustion will be used as an indicator of cardiorespiratory fitness.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in cardiorespiratory fitness assessed by a treadmill test
Description
In cases where participants do not have the opportunity to travel for physical fitness tests, cardiorespiratory fitness will be assessed by an indirect treadmill test (modified Balke protocol) at their local physiotherapist. Time to exhaustion will be used as an indicator of cardiorespiratory fitness.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in cardiorespiratory fitness assessed by a treadmill test
Description
In cases where participants do not have the opportunity to travel for physical fitness tests, cardiorespiratory fitness will be assessed by an indirect treadmill test (modified Balke protocol) at their local physiotherapist. Time to exhaustion will be used as an indicator of cardiorespiratory fitness.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in lower body muscle strength assessed by leg press
Description
The one-repetition maximum (1RM) test (the maximal workload that can be lifted once)) in leg press.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in lower body muscle strength assessed by leg press
Description
The one-repetition maximum (1RM) test (the maximal workload that can be lifted once)) in leg press.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in lower body muscle strength assessed by leg press
Description
The one-repetition maximum (1RM) test (the maximal workload that can be lifted once)) in leg press.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in upper body muscle strength assessed by push-ups
Description
The maximum number of push-ups that can be performed in one set
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in upper body muscle strength assessed by push-ups
Description
The maximum number of push-ups that can be performed in one set
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in upper body muscle strength assessed by push-ups
Description
The maximum number of push-ups that can be performed in one set
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in level of depressive symptoms assessed by the Patient Health Questionnaire-9
Description
Each of the 9 items is scored from 0-3, providing a total score from 0 to 27. A higher score implies higher level of depressive symptoms.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in level of depressive symptoms assessed by the Patient Health Questionnaire-9
Description
Each of the 9 items is scored from 0-3, providing a total score from 0 to 27. A higher score implies higher level of depressive symptoms.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in level of depressive symptoms assessed by the Patient Health Questionnaire-9
Description
Each of the 9 items is scored from 0-3, providing a total score from 0 to 27. A higher score implies higher level of depressive symptoms.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in level of anxiety symptoms assessed by the General Anxiety Disorder 7-items (GAD7).
Description
Each of the 7 items is scored from 0-3, providing a total score from 0-21. A higher score implies higher level of anxiety symptoms.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in level of anxiety symptoms assessed by the General Anxiety Disorder 7-items (GAD7).
Description
Each item is scored from 0-3, providing a total score from 0-21. A higher score implies higher level of anxiety symptoms.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in level of anxiety symptoms assessed by the General Anxiety Disorder 7-items (GAD7).
Description
Each of the 7 items is scored from 0-3, providing a total score from 0-21. A higher score implies higher level of anxiety symptoms.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Changes in sense of exercise competence assessed by the Perceived Competence Scale.
Description
The scale consists of 4 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 0 to 7 is calculated based on the mean score of the items, with increasing score implying higher exercise competence.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in sense of exercise competence assessed by the Perceived Competence Scale.
Description
The scale consists of 4 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 0 to 7 is calculated based on the mean score of the items, with increasing score implying higher exercise competence.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in sense of exercise competence assessed by the Perceived Competence Scale.
Description
The scale consists of 4 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 0 to 7 is calculated based on the mean score of the items, with increasing score implying higher exercise competence.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in satisfaction with life assessed by the Satisfaction With Life Scale.
Description
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher satisfaction with life.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Changes in satisfaction with life assessed by the Satisfaction With Life Scale.
Description
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher satisfaction with life.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in satisfaction with life assessed by the Satisfaction With Life Scale.
Description
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher satisfaction with life.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in sense of vitality assessed by the Subjective Vitality Scale
Description
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher sense of vitality.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in sense of vitality assessed by the Subjective Vitality Scale
Description
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher sense of vitality.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Changes in sense of vitality assessed by the Subjective Vitality Scale
Description
The scale consists of 5 items, each scored from 1 (totally disagree) to 7 (totally agree). A sum score from 5 to 35 is calculated, with increasing score implying higher sense of vitality.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in adherence to the Norwegian food-based dietary guidelines assessed by DIGIKOST-FFQ
Description
DIGIKOST-FFQ is a food frequency questionnaire aiming to benchmark against the Norwegian food-based dietary guidelines.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Changes in adherence to the Norwegian food-based dietary guidelines assessed by DIGIKOST-FFQ
Description
DIGIKOST-FFQ is a food frequency questionnaire aiming to benchmark against the Norwegian food-based dietary guidelines.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in adherence to the Norwegian food-based dietary guidelines assessed by DIGIKOST-FFQ
Description
DIGIKOST-FFQ is a food frequency questionnaire aiming to benchmark against the Norwegian food-based dietary guidelines.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in general health measured by European Quality of Life Five-Dimension Scale Questionnaire (EQ-5D)
Description
EQ-5D consists of five dimensions (mobility, self-care, usual activities, pain & discomfort, anxiety & depression), each of which has five severity levels that are described by statements appropriate to that dimension.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in general health measured by European Quality of Life Five-Dimension Scale Questionnaire (EQ-5D)
Description
EQ-5D consists of five dimensions (mobility, self-care, usual activities, pain & discomfort, anxiety & depression), each of which has five severity levels that are described by statements appropriate to that dimension.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in general health measured by European Quality of Life Five-Dimension Scale Questionnaire (EQ-5D)
Description
EQ-5D consists of five dimensions (mobility, self-care, usual activities, pain & discomfort, anxiety & depression), each of which has five severity levels that are described by statements appropriate to that dimension.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in quality of life among the relatives measured by Research and Development 36-term Short Form Health Survey (RAND SF-36)
Description
RAND-36 comprises 36 items that assess eight health concepts: physical functioning, role limitations caused by physical health problems, role limitations caused by emotional problems, social functioning, emotional well-being, energy/fatigue, pain, and general health perceptions. Physical and mental health summary scores are also derived from the eight RAND-36 scales.All questions are scored on a scale from 0 to 100, with 100 representing the highest level of functioning possible.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in quality of life among the relatives measured by Research and Development 36-term Short Form Health Survey (RAND SF-36)
Description
RAND-36 comprises 36 items that assess eight health concepts: physical functioning, role limitations caused by physical health problems, role limitations caused by emotional problems, social functioning, emotional well-being, energy/fatigue, pain, and general health perceptions. Physical and mental health summary scores are also derived from the eight RAND-36 scales.All questions are scored on a scale from 0 to 100, with 100 representing the highest level of functioning possible.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in quality of life among the relatives measured by Research and Development 36-term Short Form Health Survey (RAND SF-36)
Description
RAND-36 comprises 36 items that assess eight health concepts: physical functioning, role limitations caused by physical health problems, role limitations caused by emotional problems, social functioning, emotional well-being, energy/fatigue, pain, and general health perceptions. Physical and mental health summary scores are also derived from the eight RAND-36 scales.All questions are scored on a scale from 0 to 100, with 100 representing the highest level of functioning possible.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Change in quality of life among the relatives measured by the global health status / QoL scale from the European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
Description
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Time Frame
From baseline (T0) to 12 weeks (T1)
Title
Change in quality of life among the relatives measured by the global health status / QoL scale from the European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
Description
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Time Frame
From baseline (T0) to 24 weeks (T2)
Title
Change in quality of life among the relatives measured by the global health status / QoL scale from the European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).
Description
The questionnaire includes a global health status / quality of life (QoL) scale, which range in score from 0 to 100. A high score for the global health status / QoL represents a high QoL.
Time Frame
From baseline (T0) to 36 weeks (T3)
Title
Cost-effectiveness calculated based on measurements of health-related QoL and resource use (costs related to the intervention.
Description
Combining information about health-related QoL will give quality-adjusted life-years, while valuation of resource use using standard principles of health economic evaluation will provide estimates of costs
Time Frame
From baseline (0) to 36 weeks (T3)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Survivors of Hodgkin and aggressive non-Hodgkin lymphoma Not indolent non-Hodgkin lymphoma Not CNS lymphoma at diagnosis Not second cancer Not ongoing cancer treatment Chronic fatigue measured by Chalder Fatigue Questionnaire Diagnosed 2010-2020 Received treatment with curative intent 18 - 70 years old at inclusion > 2 years since last treatment Able to understand the Norwegian language Participation approval from oncologist in the project group Exclusion Criteria: Persisting fatigue > 1 year before the cancer diagnosis Somatic/physical conditions (i.e. severe heart failure/disease, lung disease, use of wheelchair /crutches) Psychiatric or mental disorders (i.e. dementia, severe depression, schizophrenia) Use of stimulants for ADHD Substance abuse disorder
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lene Thorsen, PhD
Phone
004722935181
Email
lka@ous-hf.no
First Name & Middle Initial & Last Name or Official Title & Degree
Synne-Kristin H Bøhn, PhD
Phone
004798667138
Email
synn@ous-hf.no
Facility Information:
Facility Name
Oslo University Hospital
City
Oslo
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lene Thorsen, PhD
Email
lka@ous-hf.no
First Name & Middle Initial & Last Name & Degree
Synne-Kristin Hoffart Bøhn, PhD
Phone
004798667138
Email
synn@ous-hf.no

12. IPD Sharing Statement

Learn more about this trial

A Complex Intervention for Chronically Fatigued Lymphoma Survivors

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