search
Back to results

Relaxation and Exercise In Lymphoma Patients (REIL)

Primary Purpose

Lymphoma, Quality of Life

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Exercise
Relaxation
Sponsored by
St George's, University of London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Lymphoma focused on measuring cancer survivorship, exercise, relaxation, mindfulness

Eligibility Criteria

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

Inclusion Criteria:

  1. Patients with histologically confirmed lymphoma in remission post-chemotherapy
  2. Age 18 years or older
  3. Ability to give informed consent
  4. Good Performance status (ECOG 0-2)
  5. Clinically able to carry out exercise training programme on a regular basis

Exclusion Criteria:

  1. Patients with progressive disease
  2. Poor performance status (ECOG status 3 or more)
  3. Abnormal resting ECG unexplained by further cardiological investigations
  4. Pregnancy
  5. Difficulty breathing at rest
  6. Persistent cough, fever or illness
  7. Cognitive impairment sufficient to limit ability to perform quality of life questionnaires or understand instructions

Sites / Locations

  • Haematology and Oncology Outpatient Clinic, St. George's Hospital, Blackshaw Road

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Exercise Intervention

Relaxation Intervention

Arm Description

Subjects allocated to the Exercise arm will aim to undertake a personal prescribed home exercise programme for half an hour three times a week. Exercises will be progressed at 6 weeks as subjects progress. All exercise sessions will be documented in the logbooks provided. Outcome measures will be assessed at baseline, mid-way (6 weeks) and at the end of intervention (12 weeks).

Subjects allocated to the Relaxation arm will aim to undertake a guided relaxation programme on a CD for half an hour three times a week. All relaxation sessions will be documented in the logbooks provided. Outcome measures will be assessed at baseline, mid-way (6 weeks) and at the end of intervention (12 weeks).

Outcomes

Primary Outcome Measures

Change in European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC-QLQ-C30)
The EORTC-QLQ-C30 is a self-administered questionnaire which assesses aspects of function, symptoms, and global health and QOL in samples of cancer patients. It has been demonstrated to be a valid and reliable tool in the literature, takes approximately eleven minutes to complete and most subjects require no assistance.

Secondary Outcome Measures

Change in Six Minute Walk Test distance and Heart Rate
The Six Minute Walk Test (6MWT) is a valid and reliable tool used in a variety of clinical settings, and validated for use with cancer patients. The patient is read out a set of standardised instructions to walk around a measured distance continuously as fast as they can for six minutes. Following this, the distance covered is measured and recorded, as well as their Heart Rate, Saturations, Rate of Perceived Exertion and Dyspnoea (using Borg scales) are recorded. This test gives an indication of general fitness and overall function.
Change in Grip Strength
Grip strength will be determined using hand-held dynamometry following a set of standardised guidelines. This is a common method that is used extensively to assess general strength characteristics.
Change in Spirometry values
Measures of pulmonary capacity and function including Forced Vital Capacity (FVC), Forced Expiratory Volume in one second (FEV1), Forced Expiratory Ratio (FER) and Peak Expiratory Flow (PEF) will be taken via microspirometry.
Change in FACT-Lym Questionnaire
The Functional Assessment of Chronic Illness questionnaires, have been validated in studies of cancer management and are designed to encompass the whole range of psychosocial factors. Here, the lymphoma-specific (FACT-Lym) self-administered questionaire will be used.
Change in Hospital Anxiety and Depression Scale
The Hospital Anxiety and Depression Scale (HADS) is a valid tool for the identification of psychiatric complications of cancer such as depression, anxiety or distress in cancer settings. It is a self-administered questionnaire.

Full Information

First Posted
October 16, 2014
Last Updated
February 19, 2019
Sponsor
St George's, University of London
search

1. Study Identification

Unique Protocol Identification Number
NCT02272751
Brief Title
Relaxation and Exercise In Lymphoma Patients
Acronym
REIL
Official Title
A Comparison of Exercise Training With Relaxation Intervention in Lymphoma Patients Post-chemotherapy.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
September 2014 (Actual)
Primary Completion Date
March 2017 (Actual)
Study Completion Date
March 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St George's, University of London

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will aim to compare the effects of an Exercise programme and a Relaxation Intervention in lymphoma patients in remission post-chemotherapy on quality of life, cardiovascular fitness, exercise tolerance, muscle strength, psychological status, social well-being and biological markers. Subjects will be recruited from a specialist lymphoma clinic in South West London and randomly allocated to an exercise or a relaxation home programme. The study aims to determine the more effective intervention of the two in relation to the outcome measures. The investigators anticipate that the interventions will result in less adverse events and improved quality of life and physical fitness, and subjects will require less medication, less counseling and cancer nurse specialist care, leading to leading to a reduction in hospital and surgery attendances.
Detailed Description
Significant improvements have been made in the survival rates in cancer patients. Due to factors such as screening and earlier detection of cancer and advances in treatment, cancer today is a curable disease for many. However, cancer survivors are at a significantly increased risk of morbidity and adverse effects due to treatment exposures. Commonly reported consequences of cancer treatment include fatigue, pain, depression, anxiety, reduced performance status and decreased quality of life Hence cancer today is considered more as a chronic illness, and there is increasing research being carried out on cancer survivorship and recommendations for survivorship care pathways to include interventions to enhance both physical and psychosocial functioning in cancer survivors. Previous studies have demonstrated that both exercise and interventions such as relaxation have a positive effect on both physical and psychosocial complaints of cancer survivors. These interventions are carried out in different ways, have different requirements and perceptions of the two can also be very different. No trial to date has been carried out comparing the effects of these interventions on the quality of life in cancer survivors. Furthermore, majority of the above research has been carried out on the most prevalent cancers including breast cancer, prostate cancer and colorectal cancer, and several authors have called for future research to focus on other understudied survivor groups, including haematologic cancer sites. This study aims to compare the effect of exercise and relaxation interventions on quality of life in lymphoma survivors. The aim of the present study is to compare the effects of an Exercise Intervention Program with a Relaxation Intervention in a sample of lymphoma patients in remission post-chemotherapy. Eligible subjects will be randomised to one of two arms - either an exercise or a relaxation arm. Both arms comprise of a home programme of their intervention (either exercise or relaxation) for half an hour, carried out three times a week. Subjects are assessed using the primary and secondary outcome measures at baseline, midway (6 weeks) and at the end of the intervention (12 weeks). It is hypothesised that a 12 week training programme of both exercise and relaxation would improve the quality of life of lymphoma survivors, however the exercise programme would result in a significantly greater improvement than relaxation. The null hypothesis would state that there would be no significant difference between exercise or relaxation groups following a 12 week training programme in lymphoma survivors. The aims of the study are as follows: Primary aim To compare the effectiveness of Exercise with Relaxation in the improvement of overall wellbeing and quality of life using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC-QLQ-C30). Secondary aims To determine whether these interventions result in: Improved cardio-respiratory fitness (resting HR and BP) and pulmonary function (spirometry) Improved fitness and exercise tolerance using the 6 Minute Walk Test Improved emotional and functional confidence as measured by the Health related quality of life questionnaire Functional Assessment of Cancer Therapy Lymphoma version (FACT-Lym) Decreased anxiety and depression levels using the Hospital Anxiety and Depression Scale (HADS) Changes in haematology (haemoglobin, immunoglobulins, white count) and biochemical (serum albumin, corrected calcium, creatinine) parameters Compare the results of the above outcome measures between the two interventions Analyse subject perceptions of interventions in focus groups

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphoma, Quality of Life
Keywords
cancer survivorship, exercise, relaxation, mindfulness

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise Intervention
Arm Type
Experimental
Arm Description
Subjects allocated to the Exercise arm will aim to undertake a personal prescribed home exercise programme for half an hour three times a week. Exercises will be progressed at 6 weeks as subjects progress. All exercise sessions will be documented in the logbooks provided. Outcome measures will be assessed at baseline, mid-way (6 weeks) and at the end of intervention (12 weeks).
Arm Title
Relaxation Intervention
Arm Type
Experimental
Arm Description
Subjects allocated to the Relaxation arm will aim to undertake a guided relaxation programme on a CD for half an hour three times a week. All relaxation sessions will be documented in the logbooks provided. Outcome measures will be assessed at baseline, mid-way (6 weeks) and at the end of intervention (12 weeks).
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Other Intervention Name(s)
Exercise Training
Intervention Description
The Exercise intervention will consist of aerobic activity followed by upper and lower limb resistance training using Therabands and some core exercises.
Intervention Type
Behavioral
Intervention Name(s)
Relaxation
Other Intervention Name(s)
Mindfulness
Intervention Description
The Relaxation intervention will consist of a chair-based program incorporating breathing exercises, meditation, visualisation and progressive muscle relaxation.
Primary Outcome Measure Information:
Title
Change in European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC-QLQ-C30)
Description
The EORTC-QLQ-C30 is a self-administered questionnaire which assesses aspects of function, symptoms, and global health and QOL in samples of cancer patients. It has been demonstrated to be a valid and reliable tool in the literature, takes approximately eleven minutes to complete and most subjects require no assistance.
Time Frame
Baseline, 6 weeks and 12 weeks
Secondary Outcome Measure Information:
Title
Change in Six Minute Walk Test distance and Heart Rate
Description
The Six Minute Walk Test (6MWT) is a valid and reliable tool used in a variety of clinical settings, and validated for use with cancer patients. The patient is read out a set of standardised instructions to walk around a measured distance continuously as fast as they can for six minutes. Following this, the distance covered is measured and recorded, as well as their Heart Rate, Saturations, Rate of Perceived Exertion and Dyspnoea (using Borg scales) are recorded. This test gives an indication of general fitness and overall function.
Time Frame
Baseline, 6 weeks and 12 weeks
Title
Change in Grip Strength
Description
Grip strength will be determined using hand-held dynamometry following a set of standardised guidelines. This is a common method that is used extensively to assess general strength characteristics.
Time Frame
Baseline, 6 weeks and 12 weeks
Title
Change in Spirometry values
Description
Measures of pulmonary capacity and function including Forced Vital Capacity (FVC), Forced Expiratory Volume in one second (FEV1), Forced Expiratory Ratio (FER) and Peak Expiratory Flow (PEF) will be taken via microspirometry.
Time Frame
Baseline, 6 weeks and 12 weeks
Title
Change in FACT-Lym Questionnaire
Description
The Functional Assessment of Chronic Illness questionnaires, have been validated in studies of cancer management and are designed to encompass the whole range of psychosocial factors. Here, the lymphoma-specific (FACT-Lym) self-administered questionaire will be used.
Time Frame
Baseline, 6 weeks and 12 weeks
Title
Change in Hospital Anxiety and Depression Scale
Description
The Hospital Anxiety and Depression Scale (HADS) is a valid tool for the identification of psychiatric complications of cancer such as depression, anxiety or distress in cancer settings. It is a self-administered questionnaire.
Time Frame
Baseline, 6 weeks and 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with histologically confirmed lymphoma in remission post-chemotherapy Age 18 years or older Ability to give informed consent Good Performance status (ECOG 0-2) Clinically able to carry out exercise training programme on a regular basis Exclusion Criteria: Patients with progressive disease Poor performance status (ECOG status 3 or more) Abnormal resting ECG unexplained by further cardiological investigations Pregnancy Difficulty breathing at rest Persistent cough, fever or illness Cognitive impairment sufficient to limit ability to perform quality of life questionnaires or understand instructions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ruth Pettengell, MBChB PhD
Organizational Affiliation
St George's, University of London
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ahmed Younis, PhD
Organizational Affiliation
St George's, University of London
Official's Role
Study Director
Facility Information:
Facility Name
Haematology and Oncology Outpatient Clinic, St. George's Hospital, Blackshaw Road
City
Tooting
State/Province
London
ZIP/Postal Code
SW17 0QT
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data will be submitted for publication, undecided re: individual participant data
Citations:
PubMed Identifier
32986231
Citation
Hathiramani S, Pettengell R, Moir H, Younis A. Relaxation versus exercise for improved quality of life in lymphoma survivors-a randomised controlled trial. J Cancer Surviv. 2021 Jun;15(3):470-480. doi: 10.1007/s11764-020-00941-4. Epub 2020 Sep 28.
Results Reference
derived
PubMed Identifier
31428434
Citation
Hathiramani S, Pettengell R, Moir H, Younis A. Relaxation and exercise in lymphoma survivors (REIL study): a randomised clinical trial protocol. BMC Sports Sci Med Rehabil. 2019 Aug 16;11:17. doi: 10.1186/s13102-019-0127-7. eCollection 2019.
Results Reference
derived

Learn more about this trial

Relaxation and Exercise In Lymphoma Patients

We'll reach out to this number within 24 hrs