Pilot Study of a Multigenerational Digital Lifestyle Intervention for Hispanic Female Cancer Survivors and Their Families

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this study is to assess the feasibility, acceptability, and preliminary effects of a digital (web and mobile-phone-based) program to improve lifestyle behaviors (physical activity, dietary intake) among Hispanic female cancer survivors and adult daughters.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 21
Healthy Volunteers: f
View:

• Grandmother

• Self-identifies as Hispanic

• Diagnosis of breast cancer (stages I-III), endometrial or ovarian cancer (stages I-II)

• Completed active treatment (i.e., surgery, chemotherapy, and/or radiation)

• Body Mass Index (BMI) ≥ 25 (overweight range)

• Engages in \<150 minutes/week of moderate physical activity

• English or Spanish speaking

• Owns a mobile device with internet access (e.g., smartphone, tablet)

• Lives in South Florida

• Adult daughter of the identified cancer survivor (21 years of age or older)

• Has at least 1 living child ages ≤16 years old

• Body Mass Index (BMI) ≥ 25 (overweight range) OR engages in \<150 minutes/week of moderate physical activity

• English or Spanish speaking

• Owns a mobile device with internet access (e.g., smartphone, tablet)

• Lives in South Florida

Locations
United States
Florida
University of Miami
RECRUITING
Miami
Contact Information
Primary
Vanina Pavia, MD
vxp395@miami.edu
305-243-0726
Time Frame
Start Date: 2023-02-22
Estimated Completion Date: 2026-03-01
Participants
Target number of participants: 60
Treatments
Experimental: With Love, Grandma (Con Cariño, Abuelita) Group
Cancer survivor-Daughter dyads randomized to the With Love, Grandma (Con Cariño, Abuelita) group will access a digital lifestyle program that includes 8 modules of didactic, behavioral, and family communication/parenting/grandparenting content from smartphones over the course of 10-12 weeks.
No_intervention: Control Group
This group is intended to reflect typical services cancer survivors and family members receive from healthcare providers.
Related Therapeutic Areas
Sponsors
Collaborators: The V Foundation for Cancer Research
Leads: University of Miami Sylvester Comprehensive Cancer Center

This content was sourced from clinicaltrials.gov