control: Patients in the control group will be followed with normal conventional medical treatment.
exercise: Participants in the exercise group will undergo an 8-week, 3-day-a-week exercise program.
Study summary
The aim is to investigate the effectiveness of exercise in the treatment of erectile dysfunction and premature ejaculation.
Eligibility
Sex
MALE
Min age
25 Years
Max age
45 Years
Healthy volunteers
Accepted
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
Primary outcome measure(s)
International Index of Erectile Dysfunction — 10 weeks Mean change in International Index of Erectile Dysfunction scores. There are five specific areas addressed including Erectile Function (questions:1-5 \& 15;score range: 0-5, maximum score:30); Orgasmic Function (questions:9-10; score range:0-5; maximum score:10); Sexual desire (questions:11-12; score range:1-5; maximum score:10); Intercourse satisfaction (questions:6-8; score range:0-5; maximum score:15); Overall satisfaction (questions:13-14; score range:1-5; maximum score:10). The lower the score represents greater dysfunction within each domain.
Premature Ejaculation Diagnostic Tool — 10 weeks it was developed by Symonds et al. (2007) to better define premature ejaculation for use in clinical studies, this is a 5-point Likert-type scale consisting of 5 items. The scale was adapted to Turkish by Serefoglu et al. (2009). The highest score that can be obtained from the scale is 20.0 and the lowest score is 0.0. Scores higher than 11 are defined as "Premature Ejaculation", scores of 9-10 are defined as "possible Premature Ejaculation", and scores of eight or less are defined as "no Premature Ejaculation".
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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