With Love, Grandma ("Con Cariño, Abuelita") Pilot Study for Hispanic Cancer Survivors and Daughters

This study, called "With Love, Grandma" ("Con Cariño, Abuelita"), is testing a digital program to help Hispanic women who have survived breast, endometrial (uterus), or ovarian cancer, along with their adult daughters, improve their healthy lifestyle habits like physical activity and diet. The program, delivered through smartphones and a secure website over 10-12 weeks, includes 8 modules with educational content. To join, you must be a Hispanic grandmother who has completed treatment for one of these cancers, is overweight (BMI ≥ 25), and is not very physically active. Your adult daughter would also participate. This pilot study aims to see how well the program works and how much participants like it, measured by how many mother-daughter pairs stay in the study and complete the modules. The current recruitment status is unclear.

Study design
This is an interventional study with a planned enrollment of 60 participants. It is a pilot study, meaning it's an early look at the program's potential.
What's involved
Cancer survivor-daughter pairs will log in to a secured website to access intervention content over a period of 10-12 weeks. The intervention will be delivered primarily through smartphones.
Compensation
Not stated in the trial record.
Follow-up
The primary goals of the study are measured up to 3 months after the intervention.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT05721976

With Love, Grandma ("Con Cariño, Abuelita") Pilot Study

Recruiting
NAAges 21+InterventionalTreatment
University of Miami Sylvester Comprehensive Cancer Center
~60 participants
Updated 2026-02-25 on ClinicalTrials.gov
What's tested:With Love, Grandma ("Con Cariño, Abuelita")

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percent of survivor-daughter dyads retained at post-intervention (feasibility)
Measured over Up to 3 months
+1 more outcome measured
Cancer, Breast
Cancer, Uterus
Cancer, Ovary
Obesity
Activity, Motor
Diet, Healthy
1 sites across 1 states
Florida1
  • Sara M St. George, PhD · PRINCIPAL_INVESTIGATOR · University of Miami

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

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

Exclusion

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).
Has uncontrolled schizophrenia or bipolar disorder
Has a preexisting medical condition that precludes unsupervised physical activity (e.g., severe orthopedic conditions, wheelchair bound)
  • Percent of survivor-daughter dyads retained at post-intervention (feasibility)Up to 3 months

    Calculated by percent of enrolled survivor-daughter dyads who completed post-intervention measures

  • Percent of modules completed by survivor-daughter dyads (acceptability)Up to 3 months

    Calculated as number of modules completed (of 8 total modules) by survivors and daughters