Distance-Based Exercise to Preserve Function and Prevent Disability

NCT07059884 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 104

Last updated 2026-08-05

No results posted yet for this study

Summary

This clinical trial studies whether an exercise program can be successfully delivered to patients receiving treatment for cancer through virtual sessions and allow patients to exercise in their own home. Treatments for cancer can cause side effects such as fatigue and loss of strength. These side effects can make it difficult to work, take care of family, and do other things the patient wants to do. Preliminary research shows that exercise can help prevent some of these side effects, but it can be more difficult to start an exercise program when a patient is receiving cancer treatment. The exercise program in this study is delivered through telehealth (TH) video calls. The TH sessions are delivered by trained staff that supervise resistance exercises. The trained staff also provide guidance to the patient on completing unsupervised aerobic sessions on their own. This may be a successful way to deliver an exercise program and make it easier for cancer patients to exercise in their own home during treatment.

Conditions

Interventions

OTHER

Exercise intervention

Complete supervised TH aerobic and progressive resistance exercise sessions

OTHER

Telemedicine

Complete supervised TH aerobic and progressive resistance exercise sessions

OTHER

Aerobic Exercise Intervention

Complete unsupervised aerobic exercise

OTHER

Exercise Intervention

Receive stationary bike, workbook, gloves, and resistance bands

PROCEDURE

Accelerometry

Wear accelerometer

OTHER

Questionnaire Administration

Ancillary studies

OTHER

Interview

Ancillary studies

OTHER

Electronic Health Record Review

Ancillary studies

Sponsors & Collaborators

Principal Investigators

  • Jennifer Ligibel, MD · Alliance for Clinical Trials in Oncology

  • Kathryn Schmitz, MD · Alliance for Clinical Trials in Oncology

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-11
Primary Completion
2027-07-01
Completion
2027-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07059884 on ClinicalTrials.gov