Relationships Between Physical Activity and Different Measures of Fatigue in Cancer Survivors

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-10-20

Study Completion Date

2026-06-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This is an investigation of possible relationships between daily physical activity (PA) and different measurements of fatigue in cancer survivors participating in a cancer exercise program.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Tailored Exercise Interventions to Reduce Fatigue in Cancer Survivors

NCT03049384

Cancer-related Fatigue

COMPLETED NA

Virtual Exercise Program to Reduce Cancer Related Fatigue

NCT04533165

Cancer Cancer-related Problem/Condition Fatigue

ACTIVE_NOT_RECRUITING NA

Cancer Survivors Acute Exercise Response 1

NCT03903848

Neoplasms Malignant

UNKNOWN NA

Appetite and Exercise in Breast Cancer Survivors

NCT04300478

Overweight Breast Cancer Obesity

COMPLETED NA

Telehealth Exercise Program Evaluating Fatigue and Physical Function in Rural Cancer Survivors

NCT07001241

RECRUITING PHASE2

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

This is an investigation of possible relationships between daily physical activity (PA) and different measurements of fatigue in cancer survivors participating in a cancer exercise program. Results will inform exercise prescription and timing to best reduce fatigue, as well as methodology for measuring fatigue. Participants will answer several daily questions on fatigue using a smartphone application during the 3 month exercise program and wear a PA monitor for 10 days during the first month and last month of the program.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cancer Remission

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

BfitBwell Participants

Individuals in the BfitBwell Cancer Exercise Program complete a FACIT-Fatigue questionnaire at their baseline assessment. This will be screened for all incoming BfitBwell participants and those meeting the inclusion criteria of a score of 48 or less will be approached for interest in participating. The primary research activities beyond recruitment, screening, and informed consent are the collection of EMA fatigue assessments via smartphone application and PA assessment via actigraphy.

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Be an active participant in the BfitBwell Cancer Exercise Program
* Criteria for this program include:
* Adult (\>= 18 years old)
* Being a patient seen at the University of Colorado Cancer Center
* Currently receiving cancer therapy or be within 6 months of completing cancer therapy
* Have a signed physician clearance form to participate in an exercise program
* Have a smartphone (necessary for the EMA assessments)
* A score of 48 or less on the FACIT-Fatigue (completed during the initial BfitBwell Program assessment)
* The minimally important difference of the FACIT-Fatigue is 3 points, suggesting that a score of at most 48 indicates the presence of CRF and allows for meaningful change in both directions.