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Clinical Trials/NCT05945121
NCT05945121
Recruiting
Not Applicable

Cardio-Oncology Prehabilitation Program to Improve Cardiac Reserve in High-Risk Patients Undergoing Hematopoietic Stem Cell Transplantation

University of Michigan Rogel Cancer Center1 site in 1 country10 target enrollmentAugust 25, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hematopoietic Stem Cell Transplant
Sponsor
University of Michigan Rogel Cancer Center
Enrollment
10
Locations
1
Primary Endpoint
Feasibility of a cardio-oncology prehabilitation program in high-risk HSCT candidates (adherence to program- Days).
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

To assess the feasibility and preliminary effectiveness of a Cardio-Oncology Prehabilitation program in patients at high-risk of developing Cardiovascular (CV) events in improving Cardiorespiratory fitness (CRF) and reducing acute CV complications in Hematopoietic stem cell transplant (HSCT) recipients.

Registry
clinicaltrials.gov
Start Date
August 25, 2023
End Date
August 2027
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult 18 years or older
  • Referred for HSCT evaluation
  • Presence of least one CV risk factor at enrollment (hypertension, hyperlipidemia, atrial fibrillation, obesity, heart failure, history of coronary artery disease, diabetes)
  • Able to ambulate unassisted
  • Ability to understand and the willingness to sign a written informed consent
  • Ability to use Polar Flow heart rate application

Exclusion Criteria

  • Severe anemia (hemoglobin \<7 gm/dl)
  • Untreated high-risk coronary artery disease (left main, triple vessel disease)
  • Severe aortic stenosis
  • Recent fracture as assessed via self-report
  • Gross balance deficits
  • Severe pain with basic movement
  • Unable to ambulate unassisted or exercise
  • NYHA class IV heart failure
  • Adults unable to give consent, pregnant women, and prisoners are excluded from this study.

Outcomes

Primary Outcomes

Feasibility of a cardio-oncology prehabilitation program in high-risk HSCT candidates (adherence to program- Days).

Time Frame: 8 weeks post enrollment

The percentage of days of exercised out of 24 days recommended over the 8 weeks for both aerobic and resistance activities.

Preliminary effectiveness of an 8-week cardio-oncology prehabilitation on measures of CRF in high-risk HSCT candidates (change in VO2peak).

Time Frame: 8 weeks post enrollment

change in VO2peak from pre to post intervention reported in ml/kg/min

Feasibility of a cardio-oncology prehabilitation program in high-risk HSCT candidates (Duration of Recruitment).

Time Frame: 8 weeks post enrollment

the number of participants recruited per month

Feasibility of a cardio-oncology prehabilitation program in high-risk HSCT candidates (time to implement study protocol).

Time Frame: 8 weeks post enrollment

the average amount of time required for participants to complete initial and follow-up CV assessments

Feasibility of a cardio-oncology prehabilitation program in high-risk HSCT candidates (overall satisfaction).

Time Frame: 8 weeks post enrollment

Assessed qualitatively with in-depth, semi-structured, one-to-one exit interviews with participants. A member of the research team experienced with telephone interviews, but not involved in intervention delivery, will contact all patients within 1 week after completion of the final follow-up assessment.The researcher will facilitate the interviews using a conversational-style approach whilst referring to a topic guide. Topics will focus on patients' perceived expectations, benefits, motives, and barriers to the program. The researcher will additionally ask questions regarding reasons for non-adherence to the exercise intervention, and reasons for dropout amongst discontinuing patients. The topic guide will be used flexibly to allow patients to raise additional issues which they consider important to the study. Interviews will be recorded with participants knowledge and then transcribed, coded, and assessed for relevant themes and recommendations using iterative thematic analysis

Preliminary effectiveness of an 8-week cardio-oncology prehabilitation on measures of CRF in high-risk HSCT candidates (change in anaerobic threshold).

Time Frame: 8 weeks post enrollment

change in anaerobic threshold from pre to post intervention reported in L/min

Feasibility of a cardio-oncology prehabilitation program in high-risk HSCT candidates (retention Rates).

Time Frame: 8 weeks post enrollment

percentage of enrolled participants who complete pre-post CV assessments

Feasibility of a cardio-oncology prehabilitation program in high-risk HSCT candidates (adherence to program- Time).

Time Frame: 8 weeks post enrollment

The average duration (min) of aerobic and resistance workouts over the course of the intervention.

Feasibility of a cardio-oncology prehabilitation program in high-risk HSCT candidates (Recruitment Rate).

Time Frame: 8 weeks post enrollment

Percent of eligible participants who are screened and give informed consent

Feasibility of a cardio-oncology prehabilitation program in high-risk HSCT candidates (adherence to program- Missing data).

Time Frame: 8 weeks post enrollment

the percentage of missing data from study questionnaires.

Preliminary effectiveness of an 8-week cardio-oncology prehabilitation on measures of CRF in high-risk HSCT candidates (RER).

Time Frame: 8 weeks post enrollment

change in RER (a ratio between cardiac dioxide output (VCO2)/oxygen uptake (VO2)) from pre to post intervention reported as the percent difference between the values

Preliminary effectiveness of an 8-week cardio-oncology prehabilitation on measures of CRF in high-risk HSCT candidates (comparison of V02 peak to predicted).

Time Frame: 8 weeks post enrollment

Comparison of V02 peak assessed after intervention in comparison to the predicted values reported as the percent difference between the values

Preliminary effectiveness of an 8-week cardio-oncology prehabilitation on measures of CRF in high-risk HSCT candidates (VE/VC02 slope).

Time Frame: 8 weeks post enrollment

Change in VE/VC02 slope (defined as the change in minute ventilation per unit of carbon dioxide production) from pre to post intervention

Secondary Outcomes

  • Symptom assessment scores after an 8-week cardio-oncology prehabilitation program.(8 weeks post enrollment)
  • Changes in patient reported quality of life after an 8-week cardio-oncology prehabilitation program(8 weeks post enrollment)
  • Change in patient HSCT eligibility after an 8-week cardio-oncology prehabilitation program(8 weeks post enrollment)
  • Difference in biomarkers after an 8-week cardio-oncology prehabilitation program(8 weeks post enrollment)

Study Sites (1)

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