A prospective randomized study to investigate the effect of pulsed electromagnetic field therapy on muscle mass and muscle strength in prostate cancer patients treated with androgen deprivation therapy
NCT ID NCT07057375
First seen Oct 22, 2026 · Last updated Oct 23, 2026 · Updated 1 time
Summary
This study is to assess the effect of Pulsed electromagnetic fields (PEMF) on improving muscle mass and strength in prostate cancer patients with ADT.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 110 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2025
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Male participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patients with age greater than or equal to 18 years old. * Histologically documented PCa * No evidence of distant metastasis (M1 disease) * With ADT exposure from six months to three years * Expected to continue for at least six months * At least four weeks after radical prostatectomy or completed radiotherapy Exclusion Criteria: * Patients are still under active treatment, such as radiotherapy * Patients who are unable to walk for 400 m or undertake exercise that will affect the clinical assessment of muscle strength * Patients with amputated lower limbs or other body deformities that will affect the treatment protocol
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Prince of Wales Hospital
RECRUITINGShatin, Hong Kong
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Comparison of multiparametric magnetic resonance imaging (mpMRI) versus Prostate-Specific membrane antigen positron emission tomography (PSMA-PET) for the evaluation of prostate imaging reporting and data system (PI-RADS) ≥4 lesions in the prostate transition zone: a prospective clinical study
- The investigation of new biological markers for prostate cancer diagnosis and management in chinese population
- BActinium-2: a phase 1b, 2 part, multicenter, open label study to evaluate the safety and efficacy of intravenous administration of a B7-H3 radiopharmaceutical ([225Ac]Ac AKY 2519) in participants with B7-H3 imaging positive solid tumors
- Prospective study of the effect of androgen deprivation therapy (ADT) in male patients suffered prostate cancer in asian population
- A comprehensive assessment of the physical and biological effects of patients with prostate cancer in hong kong
- A study to evaluate patient and physician benefit/ risk preferences for treatment of metastatic prostate cancer (mPC) in hong kong: a discrete choice experiment