RECRUITING

Active Living After Cancer: Implementation Within Be Well Acres Homes

Conditions

Quick Navigation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this research study is to learn more about a physical activity program adapted for cancer survivors.

Official Title

Active Living After Cancer: Implementation Within Be Well Acres Homes

Quick Facts

Study Start:2023-04-03

Study Completion:2029-04-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06907706

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Past diagnosis of invasive cancer, or a caregiver (family or friend) of a participating survivor. 2. No longer receiving treatment for cancer (except hormone therapy or long-term maintenance chemotherapy). 3. Over the age of 18. 4. Screen negative for contraindicating health problems on the adapted Physical Activity Readiness Questionnaire (PAR-Q),79 or screened positive but have approval from a health care provider to participate. 5. Lives in the Acres Homes neighborhood of Houston, Texas or has a home zip code of 77088 or 77091. 6. Able to provide informed consent.	1. Women who are pregnant (as indicated by self-report). 2. Has participated in the ALAC program within the past year and attended more than 2 group sessions.

Inclusion Criteria

Exclusion Criteria

1. Past diagnosis of invasive cancer, or a caregiver (family or friend) of a participating survivor.
2. No longer receiving treatment for cancer (except hormone therapy or long-term maintenance chemotherapy).
3. Over the age of 18.
4. Screen negative for contraindicating health problems on the adapted Physical Activity Readiness Questionnaire (PAR-Q),79 or screened positive but have approval from a health care provider to participate.
5. Lives in the Acres Homes neighborhood of Houston, Texas or has a home zip code of 77088 or 77091.
6. Able to provide informed consent.

1. Women who are pregnant (as indicated by self-report).
2. Has participated in the ALAC program within the past year and attended more than 2 group sessions.

Contacts and Locations

Study Contact

Karen Basen-Engquist, BA,MPH,PHD

CONTACT

(713) 745-3123

kbasenen@mdanderson.org

Principal Investigator

Karen Basen-Engquist, BA,MPH,PHD

PRINCIPAL_INVESTIGATOR

M.D. Anderson Cancer Center

Study Locations (Sites)

The University of Texas M. D. Anderson Cancer Center

Houston, Texas, 77090

United States

Collaborators and Investigators

Sponsor: M.D. Anderson Cancer Center

Karen Basen-Engquist, BA,MPH,PHD, PRINCIPAL_INVESTIGATOR, M.D. Anderson Cancer Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-04-03

Study Completion Date2029-04-30

Study Record Updates

Study Start Date2023-04-03

Study Completion Date2029-04-30

Terms related to this study

Additional Relevant MeSH Terms

Cancer
Fatigue