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Digital Lifestyle Intervention for Lung Cancer Survivors After Inpatient Rehabilitation (QUALUCA)

Primary Purpose

Non-Small Cell Lung Cancer (NSCLC)

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Lifestyle
Sponsored by
Kai-Uwe Schmitt, PhD, MEng, ICID
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Non-Small Cell Lung Cancer (NSCLC) focused on measuring Physical activity, Exercise, Nutrition, Breathing, Relaxation, Mobile application, Rehabilitation aftercare

Eligibility Criteria

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

Inclusion Criteria: Age ≥ 18 years Diagnosis of non-small cell lung cancer (NSCLC) Estimated life expectancy of ≥ six months (judged by health professionals) Currently undergoing inpatient rehabilitation Knowledge of German to understand study material and assessments Access to a cell phone or tablet Written informed consent Exclusion Criteria: Inability to provide informed consent due to cognitive or linguistic impairments Inability to participate in the intervention because of physical, cognitive, or safety reasons (judged by local investigators/responsible health professionals)

Sites / Locations

  • Klinik Barmelweid AGRecruiting
  • Zürcher RehaZentren | Klinik DavosRecruiting
  • Berner Reha Zentrum AGRecruiting
  • Zürcher RehaZentren | Klinik WaldRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Digital lifestyle intervention

Control

Arm Description

Self-management mobile application covering physical activity, nutrition, and breathing/relaxation

Usual care (study participation does not interfere with or change any other planned treatments)

Outcomes

Primary Outcome Measures

Health-related quality of life (Scale-Global health status)
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) (2 items; 7-point Likert-type scale; the score ranges from 0 to 100; a high score for the global health status represents a high HRQoL)

Secondary Outcome Measures

Health-related quality of life (5 functional scales, 9 symptom scales/items)
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) (28 items; 4-point Likert-type scale; 5 functional scales (physical functioning, role functioning, emotional functioning, cognitive functioning, social functioning), 3 symptom scales (fatigue, nausea and vomiting, pain), 6 single items (dyspnoea, insomnia, appetite loss, constipation, diarrhoea, financial difficulties); all scales and single-item measures range in score from 0 to 100)
Health-related quality of life (10 symptom scales/items)
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Lung Cancer 29 (lung cancer-specific module) (EORTC QLQ-LC29) (29 items; 4-point Likert-type scale / 5 multi-item scales and 5 single items; all scales and single-item measures range in score from 0 to 100)
Body mass index [kg/m²]
Computed using self-reported body weight [kg] and height [m]
Physical activity
Modified Godin-Shephard Leisure-Time Physical Activity Questionnaire (GSLTPAQ) (physical activity before inpatient rehabilitation and physical activity over the last week)
Functional exercise capacity
1-Minute Sit-to-Stand Test (number of repetitions)
Low protein intake
Protein Screener 55+ (Pro55+) (10 items)
Appetite
Simplified Nutritional Appetite Questionnaire (SNAQ) (4 items; 5-point Likert-type scale)
Psychological distress
Short form of the Patient Health Questionnaire (PHQ-4) (4 items)
Cancer-related fatigue
Brief Fatigue Inventory (BFI) (9 items)
Enablement
Shortened version of the Patient Enablement Scale-13 (PEN-13) (5 out of 13 items; 5-point Likert-type scale)

Full Information

First Posted
April 6, 2023
Last Updated
July 25, 2023
Sponsor
Kai-Uwe Schmitt, PhD, MEng, ICID
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1. Study Identification

Unique Protocol Identification Number
NCT05819346
Brief Title
Digital Lifestyle Intervention for Lung Cancer Survivors After Inpatient Rehabilitation
Acronym
QUALUCA
Official Title
Effect of a Digital Lifestyle Intervention on Health-Related Quality of Life in Non-Small Cell Lung Cancer Survivors After Inpatient Rehabilitation (QUALUCA): a Multicenter Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 2023 (Anticipated)
Primary Completion Date
November 2024 (Anticipated)
Study Completion Date
November 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Kai-Uwe Schmitt, PhD, MEng, ICID

4. Oversight

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

5. Study Description

Brief Summary
The aim of this study is to assess the efficacy of a digital lifestyle intervention in non-small cell lung cancer (NSCLC) survivors following inpatient rehabilitation on health-related quality of life (HRQoL) over three months.
Detailed Description
Lung cancer survivors suffer from reduced physical and psychological functioning as well as decreased overall health-related quality of life (HRQoL) due to cancer symptoms, cancer treatments, and comorbidities. Experienced symptoms by lung cancer survivors, such as cancer-related fatigue or dyspnea, persist after active treatment ends. Therefore, lung cancer survivors should receive continuous attention regarding their health and HRQoL beyond the expected cancer cure. Physical activity, healthy nutrition, and breathing/relaxation exercises before, during, and after cancer treatments can increase physical as well as psychological functioning and HRQoL. Thus, the adhesion to an appropriate healthy lifestyle is crucial and represents an effective adjunctive strategy in the management of lung cancer survivors. Most lung cancer survivors, however, are sedentary and fail to meet official lifestyle recommendations, for instance, of the American Cancer Society or the World Cancer Research Fund/American Institute for Cancer Research (WCRF/AICR). The present project evaluates a mobile application for non-small cell lung cancer (NSCLC) survivors that will be used for three months after inpatient rehabilitation has finished. The main foci of the mobile application are physical activity, nutrition, and breathing/relaxation. The contents of the mobile application and the mobile application itself were developed in an iterative co-creation process involving software developers and potential users as well as researchers and clinicians from different disciplines (e.g., physical therapy and nutritional therapy).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-Small Cell Lung Cancer (NSCLC)
Keywords
Physical activity, Exercise, Nutrition, Breathing, Relaxation, Mobile application, Rehabilitation aftercare

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
88 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Digital lifestyle intervention
Arm Type
Experimental
Arm Description
Self-management mobile application covering physical activity, nutrition, and breathing/relaxation
Arm Title
Control
Arm Type
No Intervention
Arm Description
Usual care (study participation does not interfere with or change any other planned treatments)
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle
Intervention Description
Participants assigned to the intervention group receive access to a lifestyle mobile application for three months after inpatient rehabilitation has finished. The digital program is target group-specific and includes personalization and interactive elements without face-to-face appointments during the intervention. One virtual appointment at the beginning of the intervention (about one week post-rehabilitation) with the study staff ensures that participants familiarize themselves with the mobile application and that they are assigned to a suitable program level. The intervention is mainly based on the following behavior change technique (BCT) clusters: goals and planning, feedback and monitoring, shaping knowledge, and comparison of behavior.
Primary Outcome Measure Information:
Title
Health-related quality of life (Scale-Global health status)
Description
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) (2 items; 7-point Likert-type scale; the score ranges from 0 to 100; a high score for the global health status represents a high HRQoL)
Time Frame
Change from baseline to 3 months
Secondary Outcome Measure Information:
Title
Health-related quality of life (5 functional scales, 9 symptom scales/items)
Description
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) (28 items; 4-point Likert-type scale; 5 functional scales (physical functioning, role functioning, emotional functioning, cognitive functioning, social functioning), 3 symptom scales (fatigue, nausea and vomiting, pain), 6 single items (dyspnoea, insomnia, appetite loss, constipation, diarrhoea, financial difficulties); all scales and single-item measures range in score from 0 to 100)
Time Frame
Change from baseline to 3 months
Title
Health-related quality of life (10 symptom scales/items)
Description
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Lung Cancer 29 (lung cancer-specific module) (EORTC QLQ-LC29) (29 items; 4-point Likert-type scale / 5 multi-item scales and 5 single items; all scales and single-item measures range in score from 0 to 100)
Time Frame
Change from baseline to 3 months
Title
Body mass index [kg/m²]
Description
Computed using self-reported body weight [kg] and height [m]
Time Frame
Change from baseline to 3 months
Title
Physical activity
Description
Modified Godin-Shephard Leisure-Time Physical Activity Questionnaire (GSLTPAQ) (physical activity before inpatient rehabilitation and physical activity over the last week)
Time Frame
Change from baseline to 3 months
Title
Functional exercise capacity
Description
1-Minute Sit-to-Stand Test (number of repetitions)
Time Frame
Change from baseline to 3 months
Title
Low protein intake
Description
Protein Screener 55+ (Pro55+) (10 items)
Time Frame
Change from baseline to 3 months
Title
Appetite
Description
Simplified Nutritional Appetite Questionnaire (SNAQ) (4 items; 5-point Likert-type scale)
Time Frame
Change from baseline to 3 months
Title
Psychological distress
Description
Short form of the Patient Health Questionnaire (PHQ-4) (4 items)
Time Frame
Change from baseline to 3 months
Title
Cancer-related fatigue
Description
Brief Fatigue Inventory (BFI) (9 items)
Time Frame
Change from baseline to 3 months
Title
Enablement
Description
Shortened version of the Patient Enablement Scale-13 (PEN-13) (5 out of 13 items; 5-point Likert-type scale)
Time Frame
Change from baseline to 3 months
Other Pre-specified Outcome Measures:
Title
Usability (intervention group only)
Description
mHealth App Usability Questionnaire (MAUQ)
Time Frame
At 3 months follow-up (end of the intervention)
Title
Acceptability, appropriateness, and feasibility (intervention group only)
Description
Acceptability of Intervention Measure (AIM), Intervention Appropriateness Measure (IAM), and Feasibility of Intervention Measure (FIM) (4-item measures of implementation outcomes)
Time Frame
At 3 months follow-up (end of the intervention)
Title
Experiences and satisfaction with the digital lifestyle intervention (intervention group only)
Description
Short semi-structured interview; outcomes will be qualitatively assessed (no scale is used)
Time Frame
At 3 months follow-up (end of the intervention)
Title
Treatments/support since baseline
Description
Cancer treatments (e.g., chemotherapy) and therapies/support (e.g., physical therapy, self-help group) participants might have received during the last 3 months (2 items)
Time Frame
At 3 months follow-up (end of the intervention)
Title
Self-rated health
Description
EuroQol Group Visual Analogue Scale (EQ VAS) (vertical visual analog scale that takes values between 100 [best imaginable health] and 0 [worst imaginable health], on which respondents provide a global assessment of their health)
Time Frame
Weekly for 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years Diagnosis of non-small cell lung cancer (NSCLC) Estimated life expectancy of ≥ six months (judged by health professionals) Currently undergoing inpatient rehabilitation Knowledge of German to understand study material and assessments Access to a cell phone or tablet Written informed consent Exclusion Criteria: Inability to provide informed consent due to cognitive or linguistic impairments Inability to participate in the intervention because of physical, cognitive, or safety reasons (judged by local investigators/responsible health professionals)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anja Frei, PhD
Phone
+41 44 634 43 60
Email
anja.frei@uzh.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anja Frei, PhD
Organizational Affiliation
University of Zurich
Official's Role
Principal Investigator
Facility Information:
Facility Name
Klinik Barmelweid AG
City
Barmelweid
ZIP/Postal Code
5017
Country
Switzerland
Individual Site Status
Recruiting
Facility Name
Zürcher RehaZentren | Klinik Davos
City
Davos
ZIP/Postal Code
7272
Country
Switzerland
Individual Site Status
Recruiting
Facility Name
Berner Reha Zentrum AG
City
Heiligenschwendi
ZIP/Postal Code
3625
Country
Switzerland
Individual Site Status
Recruiting
Facility Name
Zürcher RehaZentren | Klinik Wald
City
Wald
ZIP/Postal Code
8636
Country
Switzerland
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Digital Lifestyle Intervention for Lung Cancer Survivors After Inpatient Rehabilitation

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