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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05721976
Enrollment
60
Registered
2023-02-10
Start date
2023-02-22
Completion date
2026-12-31
Last updated
2026-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Activity, Motor, Cancer, Breast, Cancer, Ovary, Cancer, Uterus, Diet, Healthy, Obesity

Keywords

Hispanic, family, digital health, cancer survivorship, physical activity, nutrition

Brief 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.

Interventions

BEHAVIORALWith Love, Grandma ("Con Cariño, Abuelita")

Cancer survivor-Daughter dyads 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 and will include 8 modules with didactic content on healthy lifestyle behaviors for cancer prevention and control, family behavior change content for setting weekly goals and self-monitoring health behaviors, and family communication and positive parenting/grandparenting content, all of which were developed in accordance with participant feedback based on formative intervention development work. In addition, and to increase participant compliance/reduce attrition often observed in digital health interventions, human support ("supportive accountability") will be provided. Specifically, each family will be assigned a "coach" who will use video conferencing software to engage in weekly 15-30 minute sessions regarding the family's progress throughout the intervention period.

Sponsors

University of Miami Sylvester Comprehensive Cancer Center
Lead SponsorOTHER
The V Foundation for Cancer Research
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion 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

Design outcomes

Primary

MeasureTime frameDescription
Percent of survivor-daughter dyads retained at post-intervention (feasibility)Up to 3 monthsCalculated by percent of enrolled survivor-daughter dyads who completed post-intervention measures
Percent of modules completed by survivor-daughter dyads (acceptability)Up to 3 monthsCalculated as number of modules completed (of 8 total modules) by survivors and daughters

Secondary

MeasureTime frameDescription
Change in survivor and daughter physical activity as reported in the International Physical Activity Questionnaire (IPAQ)Baseline, Up to 3 monthsParticipants will self-report walking and sitting time (hours and minutes per day) using three items from the IPAQ. Mean difference in total time spent walking and sitting will be calculated from these items. The result is not reported in scales. Higher scores indicate higher time spent walking and sitting in the last 7 days.
Change in survivor and daughter physical activity as measured by the Godin Leisure Time Exercise QuestionnaireBaseline, Up to 3 monthsResponses range from 0 - greater than 24, with 0 indicating no activity and a higher score indicating more activities (no maximum score).
Change in survivor and daughter fruit and vegetable intake as measured by the NCI All-Day ScreenerBaseline, Up to 3 monthsParticipants will self-report dietary intake using the NCI All-Day Screener for fruit and vegetables and the percentage of energy from fat and fiber. Mean difference in cup equivalents of fruits and vegetables will be calculated using a scoring algorithm developed by the National Cancer Institute

Countries

United States

Contacts

CONTACTVanina Pavia, MD
vxp395@miami.edu305-243-0726
PRINCIPAL_INVESTIGATORSara M St. George, PhD

University of Miami

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026