TPS274 Background: Obese frailty is a growing national problem as trends towards aging and obesity converge. This problem is especially acute in men with prostate cancer treated with androgen deprivation therapy (ADT). ADT is essential to control advanced prostate cancer, a disease which affects mostly older men, but accelerates muscle loss and gains in adiposity which threaten physical functioning and overall quality-of-life. Diet and resistance training exercise may mitigate obese frailty but have rarely been combined in an accessible delivery format. Methods: The Internet-Based Lifestyle Intervention to Eradicate Obese Frailty in Prostate Cancer Survivors (iLIVE) Randomized Controlled Trial (RCT) aims to mitigate obese frailty among men with prostate cancer treated with ADT. Participants (N=250) are being recruited across North America to participate in this RCT that is implemented entirely over the internet. Eligibility criteria include prostate cancer history, at least 6 months of ADT in the last 10 years, body mass index ≥25 kg/m 2 and ≥2 frailty symptoms illness, fatigue, inactivity, weakness, slowness), no regular participation in strength training or on a medically-supervised diet, ability to participate in moderate intensity strength training, ability to provide informed consent, complete surveys, participate in performance testing and study interventions. Consented participants undergo assessments that include: online surveys (medical status, falls, physical activity, quality-of-life, healthcare utilization); dietary recalls (kilocalories, diet quality); body weight (Bluetooth scales); physical activity (Fitbits); 4) internet-based physical performance (chair stand, timed up-and-go, gait speed tests); and 5) muscle mass (D3 creatine dilution). Participants are then randomized to one-of-two 6-month interventions: 1) Enhanced Usual Care (EUC): Encouraged to continue Aria scale and Fitbit use with monthly emails of publicly available diet- and exercise-related information; or 2) iLIVE: Same as EUC, plus website access to weekly serialized sessions on weight loss and diet quality and thrice-weekly live remote supervised group resistance training sessions. Assessments are repeated at 6-months; at 12-months, questionnaires are repeated and data from digital devices are captured. Intent-to-treat analysis will compare EUC vs. iLIVE (baseline-to-6-months) using a composite measure of obese frailty as the primary outcome. Designed as a type I hybrid-effectiveness implementation trial, data on intervention feasibility (including safety), acceptability, adoption, appropriateness, fidelity, sustainability, and cost are assessed, tracked, and analyzed. Trial registration: ClinicalTrials.gov: NCT06011499 (5.31.2025: https://clinicaltrials.gov/study/NCT06011499). Clinical trial information: NCT06011499 .
Winters-Stone et al. (2026) studied this question.