- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07293156
Impact of Pilates Exercises on Diabetic Erectile Dysfunction. (PilatesDED2025)
Erectile dysfunction (ED) has a prevalence of 52.5% in diabetic male patients, as described in a meta-analysis of 145 studies, including 88,577 men with type 1 and type 2 diabetes.
In men, ED can cause sexual dissatisfaction and distress, unsatisfactory relationships, and marital tension
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Pilates emerged as a method of rehabilitation during World War I, when Joseph Hubertus Pilates applied his knowledge to rehabilitate injured men. The popularity of the method grew most in the 1980. More recently, Pilates has been used resulting in improved fitness (flexibility, strength and balance) and body consciousness. The method features ground-based exercises created by Joseph Pilates.
Because most Pilates exercises are performed in conjunction with the recruitment of PF muscle fibres, many Pilates instructors believe that the method can produce a significant increase in the force or contractility of the muscles. Furthermore, if Pilates promotes an improvement in the functioning of the pelvic floor muscles (PFM), it may be an alternative for the treatment and prevention of pelvic floor dysfunction.
Up till now, no published trials about impact of Pilate exercises on diabetic erectile dysfunction.
A total of 60 patients (n=30 per group), diagnosed with diabetic erectile dysfunction in the past 6 months. Participants will be recruited from Benha University hospital and local andrology and urology clinics in benha and giza . Participants will be screened for eligibility prior to being enrolled in the study participating in the study assessments.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Benha
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Banhā, Benha, Egypt
- Outpatient clinic, faculty of Physical Therapy, Benha university
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Men aged 40-60 years.
- Married.
- Diagnosed with type 2 diabetes mellitus for >5 years, with initial diagnosis confirmed by HbA1c >6.5%.
- Arteriogenic erectile dysfunction (ED) of >6 months' duration, confirmed by penile Doppler ultrasonography showing peak systolic velocity (PSV) of the cavernosal arteries <25 cm/s.
- Body mass index (BMI) <30 kg/m².
Exclusion Criteria:
- Poorly controlled diabetes mellitus (HbA1c >9%).
- Neurogenic, venogenic, or psychogenic ED.
- Cardiac conditions contraindicating sexual activity.
- Neurological disorders or spinal cord injury.
- Alcohol abuse or illicit drug use.
- Chronic hematological disorders.
- Active genitourinary infection.
- Severe hypogonadism.
- History of radical prostatectomy, pelvic surgery, or pelvic trauma.
- Penile prosthesis implantation.
- Current or previous participation in a structured pelvic floor muscle training or sexual rehabilitation program.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental
|
Pilates protocol that will be used in the present study consisted of 11 different Pilates postures: Pilates Breathing, Spine Stretch, Swan, Shoulder Bridge, Hundreds, Double Leg Stretch, Footwork, Roll up, Single Leg Stretch, Leg Pull Back, Kick front and back.
It will be performed thrice a week, with each session lasting 60 minutes, for 12 weeks, totaling 36 sessions.
The progression of the exercises will be based on increasing the number of repetitions of the exercise, and variations in posture from beginner to intermediate and advanced, for each exercise.
The movements will be repeated six to eight times each.
Participants will attend an educational session conducted by a physiotherapist on pelvic floor anatomy, the physiology of erection, and the roles of the ischiocavernosus and bulbocavernosus muscles in erectile function.
They will be instructed on proper pelvic floor muscle contraction by simulating the interruption of urine flow and performing maximal voluntary contractions.
A home-based PFMT program will be prescribed.
Exercises will initially be performed in the supine position with knees flexed and subsequently progressed to sitting or standing positions as tolerated.
Participants will be instructed to perform PFMT twice daily (morning and evening), consisting of 15 short contractions (1 second each) and 15 sustained contractions (6-10 seconds each).
Adherence will be monitored through a mobile messaging application, where participants will report completion of daily exercises and receive reminders when necessary.
Participants will receive sildenafil citrate 25 mg orally once daily and sildenafil citrate 50 mg orally on demand, taken approximately 1 hour before sexual intercourse, throughout the study period.
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Active Comparator: Active comparator
|
Participants will attend an educational session conducted by a physiotherapist on pelvic floor anatomy, the physiology of erection, and the roles of the ischiocavernosus and bulbocavernosus muscles in erectile function.
They will be instructed on proper pelvic floor muscle contraction by simulating the interruption of urine flow and performing maximal voluntary contractions.
A home-based PFMT program will be prescribed.
Exercises will initially be performed in the supine position with knees flexed and subsequently progressed to sitting or standing positions as tolerated.
Participants will be instructed to perform PFMT twice daily (morning and evening), consisting of 15 short contractions (1 second each) and 15 sustained contractions (6-10 seconds each).
Adherence will be monitored through a mobile messaging application, where participants will report completion of daily exercises and receive reminders when necessary.
Participants will receive sildenafil citrate 25 mg orally once daily and sildenafil citrate 50 mg orally on demand, taken approximately 1 hour before sexual intercourse, throughout the study period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
penile perfusion
Time Frame: Base line and after 12 weeks
|
Colour-coded duplex sonography (5-10 MHz probes) will be used for the evaluation of penile perfusion.
Half ml of a vasoactive agent (trimix solution) will be injected into the corpus cavernosum.
The systolic and diastolic velocities (cm/s) will be performed at 10 and 30 min for both cavernous artery.
Re-dosing with 0.5 ml of trimax solution will be performed for patients who did not achieve adequate hardness.
The highest values obtained will be recorded.
The Doppler indices of the right and left cavernous arteries: peak systolic velocity (PSV)
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Base line and after 12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
International Index of Erectile Function-5 (IIEF-5) scale.
Time Frame: Baseline and after 12 weeks
|
The IIEF-5 scale is used to assess patients with erectile dysfunction to determine the extent of the erectile function in patients. The full-scale 15-item version has five domains: erectile function, orgasmic function, sexual desire, intercourse satisfaction and overall sexual satisfaction. The shortened 5-item version is on a scale of 5 to 25: 22-25: No erectile dysfunction 17-21: Mild erectile dysfunction 12-16: Mild to moderate erectile dysfunction 8-11: Moderate erectile dysfunction 5-7: Severe erectile dysfunction |
Baseline and after 12 weeks
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Genital Diseases
- Endocrine System Diseases
- Mental Disorders
- Genital Diseases, Male
- Male Urogenital Diseases
- Metabolic Diseases
- Glucose Metabolism Disorders
- Sexual Dysfunction, Physiological
- Sexual Dysfunctions, Psychological
- Nutritional and Metabolic Diseases
- Diabetes Mellitus
- Erectile Dysfunction
Other Study ID Numbers
- Pilate Exercises for DED2025
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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