Clinical trial Recruiting at 1 site Interventional Ages 21 and up Women only

Digital program to improve health for Hispanic female cancer survivors and their daughters

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

Run by University of Miami · NCT05721976 · Data updated 2026-11-12

This study tests a digital program aimed at helping Hispanic female cancer survivors and their daughters improve their health habits, like exercise and diet, to see if it works well for them.

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Quick facts

Study typeInterventional
Ages21 Years and up
SexWomen only
Enrollment60 (estimated)
SponsorUniversity of Miami
Academic / other
Drugs / interventionschemotherapy, radiation
Locations1 site (Miami, Florida)
StatusRecruiting
StartedFebruary 22, 2023
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedFebruary 25, 2026
Trial IDNCT05721976 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include Hispanic grandmothers who are cancer survivors and their adult daughters, both with a BMI of 25 or higher or low physical activity levels.

Probably not a fit

Patients with distant metastatic cancer or those who do not meet the eligibility criteria will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pilot study evaluates a digital program designed to enhance lifestyle behaviors, such as physical activity and dietary intake, among Hispanic female cancer survivors and their adult daughters. The program, titled 'With Love, Grandma,' is delivered through web and mobile platforms, aiming to assess its feasibility and acceptability. Participants include grandmothers who are cancer survivors and their daughters, both of whom must meet specific health criteria. The study focuses on individuals living in South Florida who are engaged in limited physical activity.

Why it matters

Potential benefit: If successful, this program could significantly improve the health and well-being of Hispanic female cancer survivors and their daughters by promoting healthier lifestyle choices.

How similar studies have gone: Other studies focusing on digital health interventions for cancer survivors have shown promise, indicating potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Cancer Survivor Inclusion Criteria:

* 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

Daughter of Cancer Survivor Inclusion Criteria:

* 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

Daughter of Cancer Survivor Exclusion Criteria:

* Has been diagnosed with distant metastatic cancer
* Has not completed active treatment (i.e., surgery, chemotherapy, and/or radiation)
* Has uncontrolled schizophrenia or bipolar disorder
* Has a preexisting medical condition that precludes unsupervised physical activity (e.g., severe orthopedic conditions,wheelchair bound).

Cancer Survivor Exclusion Criteria:

* Has uncontrolled schizophrenia or bipolar disorder
* Has a preexisting medical condition that precludes unsupervised physical activity (e.g., severe orthopedic conditions, wheelchair bound)

Where it's running

  • University of Miami
    Miami, Florida, United States
    Recruiting

Study contacts

  • Principal investigator: Sara M St. George, PhD — University of Miami
  • Study coordinator: Vanina Pavia, MD
  • Email: vxp395@miami.edu
  • Phone: 305-243-0726

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.