The objective of this clinical trial is to evaluate the effectiveness of pelvic floor therapy for the management of erectile dysfunction and premature ejaculation in patients with erectile dysfunction and premature ejaculation. The main question to answer is: What is the effectiveness of pelvic floor therapy (electrostimulation, biofeedback, and therapeutic exercise) for the treatment of patients with erectile dysfunction and or premature ejaculation? Patients will: * Have an initial consultation of pelvic floor rehabilitation before therapy. * Be given pelvic floor therapy. * Have a secondary consultation of pelvic floor rehabilitation after therapy. Three intervention groups will be included: Group 1: Patients with premature ejaculation Group 2: Patients with erectile dysfunction Group 3: Patients with erectile dysfunction and premature ejaculation.
The objective of this clinical trial is to evaluate the effectiveness of pelvic floor therapy for the management of erectile dysfunction and premature ejaculation in patients with erectile dysfunction and premature ejaculation. Methodology: Pre-post study. Erectile function or intravaginal latency time will be evaluated before and after pelvic floor therapy, in three groups of patients, independently: * Group 1: Patients with premature ejaculation * Group 2: Patients with erectile dysfunction * Group 3: Patients with erectile dysfunction and premature ejaculation 66 patients will be included and will receive 24 sessions of pelvic floor therapy during 12 weeks. Outcomes will be evaluated at the end of therapy (12 weeks), 3 and 6 months follow-up.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
66
Recognition of the pelvic area, respiratory management, lumbo-pelvic mobilization, discrimination of abdomino-pelvic contraction and myofascial release techniques.
Free muscle work and gross motor coordination:
Muscular proprioceptive work: 50 Hz 300 µs
Boston Medical Group Colombia
Bogotá, Cundinamarca, Colombia
RECRUITINGChange in baseline intravaginal latency time (IVLT)
Change in baseline intravaginal latency time (IVLT) at the end of therapy. (Groups 1,3)
Time frame: 12 weeks
Change in International Index of Erectile Dysfuntion - Erectile Dysfunction domain (IIEF-EF) score
International Index of Erectile Dysfuntion - Erectile Dysfunction domain (IIEF-EF) score change at the end of therapy. (Groups 2,3)
Time frame: 12 weeks
Change in baseline intravaginal latency time (IVLT) at follow-up
Change in IVLT at 3 and 6 months of follow-up. (Groups 1,3)
Time frame: 3 and 6 months of follow-up.
Change Premature Ejaculation Perfil (PEP) score
Change in baseline PEP score at the end of therapy, 3 and 6 months of follow-up. (Groups 1,3)
Time frame: 12 weeks, 3 and 6 months follow-up.
Change in Premature Ejaculation Diagnosis Tool (PEDT) questionnnaire score
Change in baseline PEDT questionnaire score at the end of therapy, 3 and 6 months follow-up. (Groups 1,3)
Time frame: 12 weeks, 3 and 6 months follow-up.
Change Intracavity Assessment
Change in the parameters of the baseline Intracavity Assessment at the end of therapy, 3 and 6 months follow-up.
Time frame: 12 weeks, 3 and 6 months follow-up.
Side Effects
Incidente of side effects related to therapy.
Time frame: 12 weeks, 3 and 6 months follow-up.
Change in International Index of Erectile Dysfuntion - Erectile Dysfunction domain (IIEF-EF) score at follow-up
International Index of Erectile Dysfuntion - Erectile Dysfunction domain (IIEF-EF) score change at the 3 and 6 months of follow-up. (Groups 2,3)
Time frame: 3 and 6 months of follow-up.
Change in Erection Hardness Score (EHS)
Increase of 1 point in the baseline EHS at the end of therapy, 3 and 6 months of follow-up. (Groups 2,3)
Time frame: 12 weeks, 3 and 6 months of follow-up.
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