MD Anderson Cancer Center
Houston, Texas, 77030, United States
Location status: Recruiting
NCT Number: NCT07164456
To establish the efficacy of the family-centered intervention in improving healthy lifestyle behaviors (MVPA and overall diet quality), as well as physical functioning, QoL, and family health climate, compared to survivor-only and control groups.
Interested in participating?
Request Info18 year and older
Male
Interventional
Not applicable
Houston, Texas, 77030, United States
Location status: Recruiting
Primary Objectives
Secondary Objectives
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Eligibility Criteria
Survivors are eligible if they
Caregivers are eligible if they:
Exclusion criteria
Survivors are excluded if they:
Caregivers are excluded if they:
Remote and In person sessions
Questionnaires given a 3,6,12 mouth follow ups
Time frame: Through study completion; an average of 1 year
Contact information is provided by the study sponsor or research team.
M.D. Anderson Cancer Center
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07201805
Family Centered, Female Urogenital Diseases and Pregnancy Complications
Kahramanmaraş, Onikişubet, Turkey (Türkiye)
View Trial DetailsNCT05750316
Black Ethnicity
Reading, United Kingdom
View Trial Details