Viewing Study NCT05327452



Ignite Creation Date: 2024-05-06 @ 5:28 PM
Last Modification Date: 2024-10-26 @ 2:30 PM
Study NCT ID: NCT05327452
Status: RECRUITING
Last Update Posted: 2024-06-27
First Post: 2022-03-11

Brief Title: Testing Home-based Exercise Strategies in Underserved Minority Cancer Patients Undergoing Chemotherapy the THRIVE Study
Sponsor: Dana-Farber Cancer Institute
Organization: Dana-Farber Cancer Institute

Study Overview

Official Title: Testing Home-based Exercise Strategies to Improve Exercise Participation and Cardiovascular Health in Underserved Minority Patients With Cancer Undergoing Chemotherapy the THRIVE Study
Status: RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this research is to determine whether a 16 week home-based aerobic and resistance exercise intervention will increase physical activity levels in Black and Hispanic breast colorectal or prostate cancer patients

The names of the study interventions involved in this study are

Supervised aerobic and resistance exercise SUP - virtually supervised 16- week aerobic and resistance exercise performed at home via Zoom
Unsupervised aerobic and resistance exercise UNSUP - home-based 16- week aerobic and resistance exercise
Attention control AC - 16-week home-based stretching
Detailed Description: This is a randomized control trial of Black and Hispanic patients who have been newly diagnosed with breast colorectal or prostate cancer and are being prescribed chemotherapy to determine the effects of home-based exercise on levels of physical activity It will also evaluate the impact of home-based exercise on cardiovascular heart health risk factors

The research study procedures include screening for eligibility and study treatment including evaluations of body composition blood tests fitness and strength assessments and surveys at study entry and follow-up visits

Participants in this study will be randomly assigned to one of three groups 1 Supervised aerobic and resistance exercise SUP 2 Unsupervised aerobic and resistance exercise UNSUP or 3 Attention control AC

Participation is expected to last for 8 months

It is expected that about 135 people will take part in this research study

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
2U54CA156732-11 NIH None httpsreporternihgovquickSearch2U54CA156732-11