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NCT03880422Recruiting

Nutrition and Exercise Interventions for Androgen Deprivation Therapy-Induced Obese Frailty in Elderly and Non-Elderly Survivors of Advanced Prostate Cancer

Source: ClinicalTrials.gov · Last updated 7 May 2026

Brief summary (registry, in English)

This trial studies how well nutrition and exercise interventions work in reducing androgen deprivation therapy-induced obese frailty in prostate cancer survivors. Individualized nutrition and exercise advice for prostate cancer patients on androgen deprivation therapy may help to reduce obese frailty and change the levels of myokines in blood.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
1 Mar 2019
Start date
2 May 2019
Primary completion date
2 May 2029
Lead sponsor
Roswell Park Cancer Institute
NCT number
NCT03880422

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 2 May 2019 to the primary completion date, 2 May 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Known clinically significant severe chronic obstructive pulmonary disease (COPD), ischemic heart disease, congestive heart failure, and/or significant cardiac arrhythmias
  • Limiting orthopedic, musculoskeletal or psychological conditions (clinician discretion)
  • Any condition contraindicating additional blood collection beyond standard of care
  • Any condition which in the investigator's opinion deems the participant an unsuitable candidate to receive study intervention

Other

  • Overall medical frailty (clinician discretion)
  • Unwilling or unable to follow protocol requirements

Who the study is looking for

  • Biopsy-confirmed prostate adenocarcinoma of any stage/grade
  • Prescribed or already receiving continuous ADT for \< 5 years
  • Hemoglobin \> 11 g/dL
  • Creatinine \< 1.5 x upper limit of normal (ULN), AST or ALT \<2 x ULN within 6 months prior to enrollment
  • Liver function tests \< 2 x ULN
  • Able to walk unassisted at least 100 meters (200 steps) or ECOG \<= 1
  • No contraindications to any aspect of participation, including aerobic exercise
  • Participant must be able to read, write, and understand the English language and be able to provide written consent
  • Participant must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Roswell Park Cancer Institute
Coordinator of this site? Confirm its status
BuffaloUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.