ACTIVE_NOT_RECRUITING

Lifestyle Behavior Influences Among African American Patients With Stage 0-III Prostate Cancer Survivors and Their Partners

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

This trial studies the day-to-day stress, social support, and health lifestyle behaviors (such as physical activity and nutrition) in African American patients with stage 0-III prostate cancer survivors and their partners. How patients cope with stress may affect their lifestyle behaviors. This study may help understand not only survivors' behaviors but also partners' behaviors and how they interact.

Official Title

One Plus One Can Be Greater Than Two: Ecological Momentary Assessment for Black Prostate Cancer Survivors and Partners

Quick Facts

Study Start:2020-02-26
Study Completion:2026-02-28
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT04189770

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:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Survivors are eligible if they self-identify as African American adults
  2. * Had stage 0-III prostate cancer (no restriction on time elapsed since diagnosis)
  3. * Completed adjuvant therapy (i.e., chemo and/or radiation therapy)
  4. * Live together with a current partner/spouse who is eligible for the study
  5. * Do not need physical assistance (e.g., wheelchair, cane)
  6. * Have a smartphone
  7. * Can read and speak English
  8. * Currently are not participating in a health behavior or weight management program
  9. * Men on active surveillance will be included
  10. * Partners are eligible if they are adults
  11. * Partners are eligible if they do not have serious medical conditions (e.g., cancer, congestive heart failure, stroke, and dementia)
  12. * Partners are eligible if they have a smartphone
  13. * Partners are eligible if they can read and speak English
  14. * Partners are eligible if they currently are not participating in a health behavior or weight management program
  15. * The dyad can be either married or unmarried and same-sex or heterosexual
  1. * Survivors will be excluded if they had a prior history of other cancer or have metastatic cancer

Contacts and Locations

Principal Investigator

Dalnim Cho
PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center

Study Locations (Sites)

M D Anderson Cancer Center
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: M.D. Anderson Cancer Center

  • Dalnim Cho, 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 Date2020-02-26
Study Completion Date2026-02-28

Study Record Updates

Study Start Date2020-02-26
Study Completion Date2026-02-28

Terms related to this study

Additional Relevant MeSH Terms

  • Cancer Survivor
  • Partner
  • Spouse
  • Stage I Prostate Cancer AJCC v8
  • Stage II Prostate Cancer AJCC v8
  • Stage IIA Prostate Cancer AJCC v8
  • Stage IIB Prostate Cancer AJCC v8
  • Stage IIC Prostate Cancer AJCC v8
  • Stage III Prostate Cancer AJCC v8
  • Stage IIIA Prostate Cancer AJCC v8
  • Stage IIIB Prostate Cancer AJCC v8
  • Stage IIIC Prostate Cancer AJCC v8