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Recruiting NCT07442396

The Effectiveness of Exercise in the Treatment of Erectile Dysfunction and Premature Ejaculation

No phase Interventional Erectile Dysfunction Premature Ejaculation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: control, exercise.
Who it may be relevant to
Registry conditions: Erectile Dysfunction, Premature Ejaculation. Basic parameters: 25 years — 45 years · Male.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effectiveness of Exercise in the Treatment of Erectile Dysfunction and Premature Ejaculation: a Randomized Controlled Trial.

Overview

The aim is to investigate the effectiveness of exercise in the treatment of erectile dysfunction and premature ejaculation.

Detailed description

The study was designed as a randomized controlled trial. Participants were divided into two equal groups: a control group and an exercise group. Patients in the control group were followed with normal conventional medical treatment, while participants in the exercise group underwent an 8-week, 3-day-a-week exercise program. All participants were evaluated before and after treatment using the Index of Erectile Function, the World Health Organization Quality of Life Short Form, and the Premature Ejaculation Diagnostic Tool.

Interventions

  • Other control
    Patients in the control group will be followed with normal conventional medical treatment.
  • Other exercise
    Participants in the exercise group will undergo an 8-week, 3-day-a-week exercise program.

Primary outcome measures

  • International Index of Erectile Dysfunction [Time frame: 10 weeks]
  • Premature Ejaculation Diagnostic Tool [Time frame: 10 weeks]

Eligibility criteria

Inclusion criteria

  • Male individuals aged 25-45 years
  • Individuals diagnosed with erectile dysfunction and premature ejaculation
  • Individuals who voluntarily agree to participate in the study and sign the informed consent form
  • Individuals who have the physical and cognitive capacity to participate in pelvic floor physiotherapy applications

Exclusion criteria

  • Individuals with a history of surgery in the pelvic region
  • Individuals with a diagnosis of neurological disease or neurological disorder that may affect pelvic floor muscle function
  • Presence of active infection, inflammation, or painful pathology in the pelvic region
  • Individuals who regularly use medications that significantly affect sexual function
  • Individuals with serious psychiatric illness or cognitive impairment that may hinder study compliance

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Turkey (Türkiye) · 1 center
  • Uskudar university — Istanbul

Publications

  • Yaacov D, Nelinger G, Kalichman L. The Effect of Pelvic Floor Rehabilitation on Males with Sexual Dysfunction: A Narrative Review. Sex Med Rev. 2022 Jan;10(1):162-167. doi: 10.1016/j.sxmr.2021.02.001. Epub 2021 Apr 27. PMID 33931383
  • Sahin E, Brand A, Cetindag EN, Messelink B, Yosmaoglu HB. Pelvic physical therapy for male sexual disorders: a narrative review. Int J Impot Res. 2025 Dec;37(12):941-949. doi: 10.1038/s41443-025-01034-5. Epub 2025 Feb 27. PMID 40016382
  • Niu C, Ventus D, Wen G, Santtila P. Associations between self-reports of physical activity, interoceptive awareness, autonomic regulation, premature ejaculation, and erectile dysfunction in Chinese men. Int J Impot Res. 2025 Dec;37(12):992-1001. doi: 10.1038/s41443-025-01072-z. Epub 2025 Apr 19. PMID 40251377

Identifiers

NCT: NCT07442396 · Uskudar93

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗