- 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 (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Mahmoud Hamada Mohamed Associate Professor, Ph.D
- Phone Number: 01096968910
- Email: mahmoud.mohamed@fpt.bu.edu.eg
Study Locations
-
-
Benha
-
Banhā, Benha, Egypt
- Recruiting
- Outpatient clinic, faculty of Physical Therapy, Benha university
-
Contact:
- Mahmoud Hamada Mohamed Associate Professor, Ph.D
- Phone Number: 01096968910
- Email: mahmoud.mohamed@fpt.bu.edu.eg
-
Contact:
- Ahmed Mounir Salama Associate Professor, Ph.D
- Phone Number: 0109393961
- Email: ahmed.moumir@fpt.bu.edu.eg
-
-
Giza Governorate
-
Giza, Giza Governorate, Egypt
- Withdrawn
- Outpatient clinic, faculty of Physical Therapy, Ahram Canadian university
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Men aged 40-60 years.
- Diagnosed diabetes mellitus (type 2) ≥ 1 year.
- Clinical diagnosis of erectile dysfunction for ≥ 6 months, confirmed by IIEF5 score.
- Stable antidiabetic medications for ≥ 3 months prior to randomization.
- HbA1c between 6.5% and 10.0%.
- Sexually active or attempting sexual activity at least occasionally (at least once monthly) and willing to attempt intercourse during study.
- Able and willing to participate in the exercise program (physically capable and available for scheduled sessions) and provide written informed consent.
Exclusion Criteria:
- Severe cardiovascular disease within past 6 months (e.g., recent myocardial infarction, unstable angina, decompensated heart failure, uncontrolled arrhythmia) that contraindicates exercise.
- Uncontrolled hypertension (e.g., systolic ≥ 180 mmHg or diastolic ≥ 110 mmHg) despite treatment.
- Severe peripheral vascular disease or other conditions preventing safe exercise (severe claudication, severe orthopedic limitations).
- History of pelvic surgery or pelvic radiation within the last 12 months that could acutely affect erectile function.
- Primary neurogenic causes of ED unrelated to diabetes (spinal cord injury, multiple sclerosis).
- Major psychiatric illness or severe cognitive impairment interfering with consent/compliance .
- Current substance abuse or heavy alcohol use that could affect sexual function or compliance.
- Severe hypogonadism requiring imminent testosterone therapy (total testosterone < 8 nmol/L with symptoms).
- Active genitourinary infection or untreated severe sexual dysfunction disorders other than ED.
- Use of medications known to cause ED that cannot be discontinued or stabilized.
- Current participation in structured pelvic floor or sexual-function exercise program similar to the intervention.
- Recent (within 4 weeks) or planned changes in PDE5i therapy.
- Any medical condition making participation unsafe or likely to confound outcomes per investigator judgment.
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
study group
|
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.
The pelvic floor exercises will be taught by a skilled physiotherapist who instructed the men to tighten their pelvic floor muscles as strongly as possible (as if to prevent flatus from escaping), to gain muscle hypertrophy. During pelvic floor muscle training attention was placed on the ability to retract the penis and lift the scrotum, to make sure the bulbocavernosus and ischiocavernosus muscles were working strongly. Emphasis was placed on gaining a few maximum contractions (three when lying, three sitting, and three standing) twice daily rather than prolonged repetitions. Some submaximal pelvic floor work will be advised while walking, to increase muscle endurance. Men will be also taught to tighten their pelvic floor muscles strongly after voiding urine whilst still poised over the toilet, as a way of working the bulbocavernosus muscle to eliminate the urine from the bulbar urethra. Frequency of treatment: Treatment will be given 3 times / week for 12 weeks total of 36 session |
|
Active Comparator: Active comparator
control
|
The pelvic floor exercises will be taught by a skilled physiotherapist who instructed the men to tighten their pelvic floor muscles as strongly as possible (as if to prevent flatus from escaping), to gain muscle hypertrophy. During pelvic floor muscle training attention was placed on the ability to retract the penis and lift the scrotum, to make sure the bulbocavernosus and ischiocavernosus muscles were working strongly. Emphasis was placed on gaining a few maximum contractions (three when lying, three sitting, and three standing) twice daily rather than prolonged repetitions. Some submaximal pelvic floor work will be advised while walking, to increase muscle endurance. Men will be also taught to tighten their pelvic floor muscles strongly after voiding urine whilst still poised over the toilet, as a way of working the bulbocavernosus muscle to eliminate the urine from the bulbar urethra. Frequency of treatment: Treatment will be given 3 times / week for 12 weeks total of 36 session |
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 following Doppler indices of the right and left cavernous arteries: peak systolic velocity (PSV), end-diastolic velocity (EDV) and resistance index (RI) will be recorded.
|
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
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
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