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Cancer Rehab Program for Allogenic Bone and Marrow Transplant Patients - CaRE-4-alloBMT

Primary Purpose

Allogeneic Disease, Hematologic Cancer, Cancer Rehabilitation

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
CaRE-4-alloBMT plus usual care group
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Allogeneic Disease

Eligibility Criteria

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

Inclusion Criteria:

  • 18 years of age or older
  • Must have received a hematologic cancer diagnosis
  • Awaiting alloBMT
  • Able to communicate in English
  • Able to access online study material (Physitrack and education e-modules).

Exclusion Criteria:

  • Not meeting the inclusion criteria

Sites / Locations

  • Princess Margaret Cancer Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Usual care group

CaRE-4-allBMT plus usual care

Arm Description

No change to patient's usual care at Princess Margaret Cancer Centre.

a longitudinal 6-month rehabilitation program that uses a person- centred strategy and a multidimensional approach targeting physical activity, nutrition, psychosocial distress and promoting self-management skills.

Outcomes

Primary Outcome Measures

Drop-out rates as a measure of feasibility
Number of patients who complete the study/ drop-out will be used to identify feasibility of the intervenion.
Patient preference as assessed during clinical support as a measure of feasibiity
Check-ins with health coach during assessments will be used to identify intervention acceptability/preference.
Measuring safety as assessed during one-on-one interviews with health coach - this wll be (analyzed as qualitative data) done over MS Teams and will be a conversational question and answer format.
Patients will be checking-in at specific timepoints with a health coach to discuss their preference/challenges with intervention.

Secondary Outcome Measures

Disability assessment schedule
World Health Organization Disability Assessment Schedule 2.0. The scale is (0-4) for a total score from 0-48 and the larger the value the worse the outcome.
36 items short form health survey
self reported measure of overall health - total score: 0-100 and the higher the score, the better the health state (less disability)
Evaluating nutritional status based on caloric intake
using data from fitbit worn by patient to record their daily caloric intake.
Using the Body Mass Indext to measure nutritional status
Body Mass Index
Measure of nutritional status by using the Patient Generated Subjective Global Assessment
Patient-reported instrument for assessment of nutrition status in patients with cancer - Typical scores range from 0-35 with a higher score reflecting a greater risk of malnutrition and scores ≥9 indicating a critical need for nutrition intervention and symptom management.
General Anxiety Disorder assessment
Measure of General Anxiety and distress - total score: 0-21 and the cut-offs are: 0-4: minimal anxiety 5-9: mild anxiety 10-14: moderate anxiety 15-21: severe anxiety
Functional Assessment of Cancer Therapy for Bone Marrow Transplant
a measure of quality of life - total score of 0-196 with a higher scores for the scales and subscales indicate better quality of life.
Measure of the level of healthcare utilization by patient
clinic chart details for days in hospital, readmission
measure of overall survival
will be interpretted from the quantitative and qualitative date extracted
Euroqol 5D
Health related quality of life - The maximum score of 1 indicates the best health state, by contrast with the scores of individual questions, where higher scores indicate more severe or frequent problems.
6 minute walk test
measures the distance an individual is able to walk over a total of six minutes on a hard, flat surface
grip strength tests
measures the muscular strength or the maximum force/tension generated by one's forearm muscles
Sit-to-stand test
measurement that assesses functional lower extremity strength in older adults

Full Information

First Posted
April 26, 2021
Last Updated
May 7, 2023
Sponsor
University Health Network, Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT04966156
Brief Title
Cancer Rehab Program for Allogenic Bone and Marrow Transplant Patients - CaRE-4-alloBMT
Official Title
A Longitudinal Multidimensional Cancer Rehab Program for Patients Undergoing Allogenic Bone and Marrow Transplantation (CaRE-4-alloBMT)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
September 8, 2021 (Actual)
Primary Completion Date
November 30, 2022 (Actual)
Study Completion Date
January 31, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto

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
Currently, transplantation centers across North America generally do not offer longitudinal rehabilitation programs and research is urgently needed to test the acceptability and effectiveness of these programs using innovative delivery strategies that have the potential for future scalability and to understand the associated costs. Through a strong collaboration between the PM Cancer Rehabilitation and Survivorship (CRS) and alloBMT teams, the principal investigators developed an innovative multicomponent rehabilitation intervention for patients undergoing alloBMT (CaRE-4-alloBMT). CaRE-4-alloBMT uses a person- centred strategy and a multidimensional approach targeting physical activity, nutrition, psychosocial distress and promoting self-management skills. Innovative components of CaRE-4-alloBMT include:1) Individualized progressive exercise prescriptions developed and monitored by CRS registered kinesiologists and supported with a web/mobile application (Physitrack) that allows customizable exercise prescriptions, tracking of exercise completion, and video tutorials; 2) Individualized nutrition plans and stepped stratified care (education, counselling, intervention) based on nutritional status and delivered by registered dietitians (alloBMT and CRS). 3) On-line e-modules (developed in collaboration with PM Oncology Education) provide interactive education to promote self-management skills on crucial topics; 4) Remote monitoring using FitbitTM devices to monitor patients physical activity, caloric intake, and sleep for duration of the program; 5) Remote clinical support: Pre/Post discharge, patients will have scheduled (PHS) remote check-ins and health coaching sessions with a member of the CRS team (phone or MS Teams video). Objectives: i) To test the feasibility and safety of CaRE-4-alloBMT plus standard best practice cancer care compared to standard best practice cancer care alone; ii) To assess the preliminary efficacy of CaRE-4-alloBMT on physical function, disability, nutritional status, distress, QoL, healthcare utilization, and survival and estimate program return on investment.
Detailed Description
1.0 BACKGROUND: Allogeneic blood and marrow transplantation (alloBMT) is a curative treatment for many hematologic cancers and its use has increased rapidly over the past decade. While effective, alloBMT is associated with numerous treatment-related physical and psychosocial side effects, reduced physical functioning, and worsening nutritional status which are associated with increased risk of complications (i.e. infections, drug toxicity, weight loss, graft failure & graft-versus-host disease), significant early and late treatment related mortality, and can profoundly affect quality of life (QoL). As a result, there have been calls for increased attention to the management of adverse effects associated with alloBMT with the goal to minimize dysfunction, maximize well-being and QoL, and reduce treatment-related mortality. Cancer rehabilitation is now considered an essential component of cancer care and focuses on prevention and treatment of the adverse effects of cancer and treatment and to optimize functional status and QoL. Embedding multidimensional longitudinal (pre to post transplant) rehabilitation programs that focus on exercise, nutrition and teaching self-management skills as a standard part of treatment for individuals undergoing alloBMT has potential to mediate the significant adverse effects, improve survival, and reduce burden on the healthcare system. While patients typically receive some in-patient rehabilitation, this is a small part of the alloBMT pathway and services are quite limited. Currently, transplantation centers across North America generally do not offer longitudinal rehabilitation programs and research is urgently needed to test the acceptability and effectiveness of these programs using innovative delivery strategies that have the potential for future scalability and to understand the associated costs. In response, through a strong collaboration between the PM Cancer Rehabilitation and Survivorship (CRS) and alloBMT teams, the principal investigators developed an innovative multicomponent rehabilitation intervention for patients undergoing alloBMT (CaRE-4-alloBMT). 2.0 PROGRAM DESCRIPTION (see Appendix 1): CaRE-4-alloBMT is a longitudinal 6-month rehabilitation program (peri to post transplant) adapted from an existing evidence-based and effective model developed by the CRS team (CaRE@ELLICSR and CaRE@Home). The program is informed by established behaviour change theory and harnesses current and emerging eHealth technologies to reduce barriers to accessing and providing cancer rehabilitation. CaRE-4-alloBMT uses a person- centred strategy and a multidimensional approach targeting physical activity, nutrition, psychosocial distress and promoting self-management skills. Innovative components of CaRE-4-alloBMT include: Individualized progressive exercise prescriptions developed and monitored by CRS registered kinesiologists and supported with a web/mobile application (Physitrack) that allows customizable exercise prescriptions, tracking of exercise completion, and video tutorials. The initial personalized exercise program will be given to a participant following the initial assessment. A program will be created based on the specific needs and physical condition of each participant. The participant will receive the detailed exercise program via Physitrack (includes exercise description and videos of each exercise). Each exercise program will contain cardiovascular and strength training as well as stretching exercises. The exercise program will be revised and progressions will be added based on the individual's needs after the follow-up assessments or during the scheduled check-ins between assessments. Check-ins are scheduled as follows: At 2 and 4 weeks after initial assessment 8 weekly check-ins following discharge At 10 and 12 weeks following discharge The participant can contact the Kinesiologist by e-mail at any point during the program. Individualized nutrition plans and stepped stratified care (education, counselling, intervention) based on nutritional status and delivered by registered dietitians (alloBMT and CRS). As part of standard of care, all patients receive a nutrition assessment and their caloric intake goals are set. Those in the INT arm (CaRE-4-alloBMT plus usual care group) will receive additional nutritional education through the e-modules and monitoring of caloric intake through the Fitbit. They will also have access to meal preparation and recipes through ellicsrkitche.ca. Patients can track their nutritional intake on their Fitbit device and this data will be monitored weekly by the RKin. Patients who falls below 50% of their goals (based on intake assessment) will flagged to the RD for follow up. On-line e-modules (developed in collaboration with PM Oncology Education) provide interactive education to promote self-management skills on crucial topics (i.e. stress management, nutrition, managing common symptoms). There will be 9 online e-modules: Introduction: Getting started Eat and Cook for Wellness Exercise Manage Your Emotions Reduce Fatigue Being Mindful Boost Your Brain Health Stay Connected Planning for the Future Participants will be asked to complete all 9 modules. Each module should take between 20-30 minutes to complete. Participants can go through these modules at their own pace. Patients will receive a link for the online modules. Patients will be able to access the module by entering their e-mail address and creating their own unique password. Remote monitoring using FitbitTM devices to monitor patients physical activity, caloric intake, and sleep for duration of the program. CRS and alloBMT clinicians will have access to real-time Fitbit data through the clinical dashboard (developed in collaboration with TECHNA). The Fitbit is also known to promote behaviours change and allows for self-monitoring and feedback. Participants will be asked to wear the Fitbit for the duration of the study. Participants will only need to add their meals to monitor their nutrition. No other action is required from the participants once the account has been created. This will replace the paper based food diary they must keep (standard of care). The account for the participant will be created by the RA or RKin and the participant will then be able to access the app via an email link. The RA or RKin can assist/provide support to the participant as needed to access the app. If the participant is unable to download or use the app a detailed print out of their exercise program will be provided. The following information will be required to create an account: First name Last name (participant study number will be entered in this field Year of birth Email address Both the participant and Kinesiology team will have access to this information but the account information is not visible to third parties. Physitrack provides links to the privacy policy and terms of use/agreement and is available for the participant to review as needed. Remote clinical support: Pre/Post discharge, patients will have scheduled (PHS) remote check-ins and health coaching sessions with a member of the CRS team (phone or MS Teams video). These occur in week 2,4 (pre) and 1-8,10,12 (post-discharge). Frequency of check-ins and what will be discussed: Check-ins are by telephone or MSteams video and scheduled as follows: At 2 and 4 weeks after initial assessment (pre-BMT admission) Weeks 1-8, 10 and 12 post-discharge (post-BMT dischange) - Check-ins discussion using motivational interviewing techniques and focus on Adherence to exercise program Changes to exercise program based on participant's needs Module completion Answering participants questions The program strongly aligns with the SUNDAE framework

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allogeneic Disease, Hematologic Cancer, Cancer Rehabilitation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be informed when consented that they will be grouped into one of two (control or intervenion) study groups for the duration of the study. Following their baseline assessment, patients will be randomized (1:1 stratified by age and clinical frailty score at pre-transplant consultation).
Masking
Participant
Masking Description
biostatician will provide the randomized grouping for each of the participants.
Allocation
Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Usual care group
Arm Type
No Intervention
Arm Description
No change to patient's usual care at Princess Margaret Cancer Centre.
Arm Title
CaRE-4-allBMT plus usual care
Arm Type
Experimental
Arm Description
a longitudinal 6-month rehabilitation program that uses a person- centred strategy and a multidimensional approach targeting physical activity, nutrition, psychosocial distress and promoting self-management skills.
Intervention Type
Behavioral
Intervention Name(s)
CaRE-4-alloBMT plus usual care group
Intervention Description
CaRE-4-alloBMT uses emerging eHealth technologies to reduce barriers to accessing and providing cancer rehabilitation which includes: 1) Individualized progressive exercise prescriptions that allows customizable exercise prescriptions, tracking of exercise completion, and video tutorials; 2) Individualized nutrition plans and stepped stratified care such as education, counselling, intervention based on nutritional status and delivered by registered dietitians; 3) On-line e-modules provide interactive education to promote self-management skills for stress management, nutrition, managing common symptoms, etc.; 4) Remote monitoring using FitbitTM devices to monitor patients physical activity, caloric intake, and sleep for duration of the program. CRS and alloBMT clinicians will have access to real-time Fitbit data through our clinical dashboard; 5) Remote clinical support: check-ins and health coaching sessions with a member of the CRS team (phone or MS Teams video).
Primary Outcome Measure Information:
Title
Drop-out rates as a measure of feasibility
Description
Number of patients who complete the study/ drop-out will be used to identify feasibility of the intervenion.
Time Frame
6 months
Title
Patient preference as assessed during clinical support as a measure of feasibiity
Description
Check-ins with health coach during assessments will be used to identify intervention acceptability/preference.
Time Frame
6 months
Title
Measuring safety as assessed during one-on-one interviews with health coach - this wll be (analyzed as qualitative data) done over MS Teams and will be a conversational question and answer format.
Description
Patients will be checking-in at specific timepoints with a health coach to discuss their preference/challenges with intervention.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Disability assessment schedule
Description
World Health Organization Disability Assessment Schedule 2.0. The scale is (0-4) for a total score from 0-48 and the larger the value the worse the outcome.
Time Frame
6 months
Title
36 items short form health survey
Description
self reported measure of overall health - total score: 0-100 and the higher the score, the better the health state (less disability)
Time Frame
6 months
Title
Evaluating nutritional status based on caloric intake
Description
using data from fitbit worn by patient to record their daily caloric intake.
Time Frame
6 months
Title
Using the Body Mass Indext to measure nutritional status
Description
Body Mass Index
Time Frame
6 months
Title
Measure of nutritional status by using the Patient Generated Subjective Global Assessment
Description
Patient-reported instrument for assessment of nutrition status in patients with cancer - Typical scores range from 0-35 with a higher score reflecting a greater risk of malnutrition and scores ≥9 indicating a critical need for nutrition intervention and symptom management.
Time Frame
6 months
Title
General Anxiety Disorder assessment
Description
Measure of General Anxiety and distress - total score: 0-21 and the cut-offs are: 0-4: minimal anxiety 5-9: mild anxiety 10-14: moderate anxiety 15-21: severe anxiety
Time Frame
6 months
Title
Functional Assessment of Cancer Therapy for Bone Marrow Transplant
Description
a measure of quality of life - total score of 0-196 with a higher scores for the scales and subscales indicate better quality of life.
Time Frame
6 months
Title
Measure of the level of healthcare utilization by patient
Description
clinic chart details for days in hospital, readmission
Time Frame
6 months
Title
measure of overall survival
Description
will be interpretted from the quantitative and qualitative date extracted
Time Frame
6 months
Title
Euroqol 5D
Description
Health related quality of life - The maximum score of 1 indicates the best health state, by contrast with the scores of individual questions, where higher scores indicate more severe or frequent problems.
Time Frame
6 months
Title
6 minute walk test
Description
measures the distance an individual is able to walk over a total of six minutes on a hard, flat surface
Time Frame
6 months
Title
grip strength tests
Description
measures the muscular strength or the maximum force/tension generated by one's forearm muscles
Time Frame
6 months
Title
Sit-to-stand test
Description
measurement that assesses functional lower extremity strength in older adults
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years of age or older Must have received a hematologic cancer diagnosis Awaiting alloBMT Able to communicate in English Able to access online study material (Physitrack and education e-modules). Exclusion Criteria: Not meeting the inclusion criteria
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer M Jones, PhD
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Princess Margaret Cancer Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C1
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

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Cancer Rehab Program for Allogenic Bone and Marrow Transplant Patients - CaRE-4-alloBMT

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