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Decreasing Cardiometabolic Risk in Childhood Cancer Survivors: The STRENGTH (Survivors Engaged in Time-Restricted EatiNG After THerapy) Study

NCT ID: NCT07009288Sponsor: Memorial Sloan Kettering Cancer CenterLast updated: 2026-05-27

Summary

This study will look at whether motivational sessions (including regular calls with a trained health coach) in combination with time-restricted eating (TRE) is an effective way to achieve weight loss and lower cardiometabolic risk in adult survivors of childhood cancer. The researchers will look at how effective this intervention is compared to the usual approach, which is to review educational materials and measure weight once a month. This study will not provide treatment for any disease or cancer.

Arms & interventions

  • OtherChildren's Oncology Group Heart Health Link

    Educational materials on healthy lifestyle behaviors.

  • OtherMonthly weights

    Weight (kg): measured remotely via Withings Body + scale, Height, weight, waist circumference, BP, and % body fat

  • OtherFasting

    (14-hour fast x 2 weeks; 15-hour fast x- 1 week; 16-hour fast for the remainder of the active intervention)

  • OtherCalls

    Month 1-3: Bi-weekly call using motivational interviewing Months 4-6: Monthly call using motivational interviewing Support via SMS text

  • OtherParticipant Questionnaires

    Questions on worry, perceived self-efficacy, health beliefs and knowledge of late effects (adapted from EQUAL study), Behavioral Risk Factor Surveillance System, Physical Activity Questionnaire, Link to Automated Self-Administered 24-Hour (ASA24) Dietary Assessment Tool with accompanying sleep module

  • OtherDried blood spot

    Glucose, insulin, hemoglobin A1c, lipids. Measured remotely in the fasting state via dried blood spots in the participant's home.

Outcome measures

Primary

  • Percent change in weight

    Time frame: at 12 months

Secondary

  • Change in glucose

    Time frame: up to 12 months

  • Change in insulin

    Time frame: up to 12 months

  • Change in HbA1c

    Time frame: up to 12 months

Eligibility criteria

Sex: AllAge: 18 Years and olderHealthy volunteers: No
Inclusion Criteria: * Enrolled in the Childhood Cancer Survivor Study (a cohort of 5+ year survivors of childhood cancer diagnosed at age \< 21 between 1970-1999 at 31 participating institutions in North America) * Are ≥18 years old * Self-reported body mass index ≥ 25 kg/m2 * Are not pregnant or do not intend to become pregnant in the next year * Stable weight over the past 3 months (+/- 10 pounds) * If on oral medication for insulin resistance (ie, metformin), elevated blood pressure, or dyslipidemia, medication dose must be stable (ie, unchanged \> 3 months) * Have internet access (can be via smartphone or computer). If neither device is available, the study can loan participants a Wi-Fi enabled device. Exclusion Criteria: * Do not reside in the United States * Do not speak English * Eating window \< 12 hours per 24-hour day * On insulin or GLP-1 agonist * Diagnosis of type 1 diabetes mellitus * Enrolled in a formal weight management program or other weight loss trial * History of an eating disorder

Study locations (4)

Hunter College

New York, New York, 10065

Not Yet Recruiting
Jennifer Ford, PhD · Contact
Jennifer Ford, PhD · Principal Investigator

Memorial Sloan Kettering Cancer Center

New York, New York, 10065

Recruiting
Danielle Friedman, MD · Contact
Chaya Moskowitz, PhD · Contact
Danielle Friedman, MD · Principal Investigator

St. Jude Children's Research Hospital (Data Collection Only)

Memphis, Tennessee, 38105

Recruiting
Gregory Armstrong, MD · Contact
Gregory Armstrong, MD · Principal Investigator

Fred Hutchinson Cancer Research Center (Data Collection Only)

Seattle, Washington, 98109

Not Yet Recruiting
Mary Kwok, MD · Contact