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NCT07064811Not yet recruiting

Standardized Resistance Training Program and Assessment System for Prostate Cancer Patients Receiving Androgen Deprivation Therapy ISPoRT-PCa-ADT Study Protocol for a Randomized Controlled Trial. SPORT-MU

Source: ClinicalTrials.gov · Last updated 15 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This randomized controlled trial (RCT) with two parallel study arms evaluated the effectiveness of a 24-week exercise intervention in prostate cancer (PCa) patients under-going androgen deprivation therapy (ADT). Ethical approval was obtained from the Clinical Research Ethics Committee of the University Clinical Hospital "Virgen de la Arrixaca" (Murcia, Spain). Participants were randomly assigned to one of two groups: (1) a supervised progressive resistance training program (SPoRT-PCa-ADT), or (2) a control group receiving a home-based exercise protocol following an initial assessment, accom-panied by weekly telephone follow-up. Assessments were conducted at baseline and at 24 weeks to examine changes in physical, functional, and psychosocial outcomes. Addi-tionally, patient-reported outcomes were collected at the 12-week midpoint (Figure 1). This study design enabled the evaluation of both immediate and sustained intervention effects and facilitated a direct comparison between supervised and home-based exercise approaches

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
7 Jul 2025
Start date
15 Nov 2025
Primary completion date
15 Feb 2027
Lead sponsor
Fundacion para la Formacion e Investigacion Sanitarias de la Region de Murcia
NCT number
NCT07064811

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 15 Nov 2025 to the primary completion date, 15 Feb 2027
  • 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

  • no controlled or symptomatic metastatic bone disease

Other

  • unwillingness to participate in the study
  • inability to complete adequate follow-up due to any cause that would prevent knowledge of patient evolution during the follow-up period
  • physical disabilities that would prevent participants from safely completing the exercise protocol

Who the study is looking for

  • diagnosis of locally advanced or metastatic prostate neoplasm and current treatment with androgen deprivation therapy (ADT)
  • treatment at the radiotherapy oncology department of University Clinical Hospital "Virgen de la Arrixaca"
  • legal adult age with signed informed consent

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
HCUVA
Coordinator of this site? Confirm its status
MurciaSpainUnknown status

Related publications

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