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Lifestyle Modification for Erectile Dysfunction in Men With Metabolic Syndrome (LIFE-MetS-ED)

13 de agosto de 2026 actualizado por: Abul-fotouh Ahmed, Al-Azhar University

Penile Hemodynamic Recovery Following a Six-Month Structured Lifestyle Modification Program in Men With Metabolic Syndrome-Associated Erectile Dysfunction: A Prospective Single-Arm Interventional Study

Metabolic syndrome is associated with erectile dysfunction through obesity, insulin resistance, abnormal blood lipids, high blood pressure, and impaired blood-vessel function. This study will evaluate whether a structured six-month lifestyle-modification program can improve penile blood flow and erectile function in men with metabolic syndrome-associated erectile dysfunction.

Eligible participants will receive dietary counseling, exercise guidance, weight-management advice, smoking-cessation counseling when applicable, sleep and sedentary-behavior advice, and repeated behavioral reinforcement. Erectile function, penile blood-flow measurements obtained by penile duplex Doppler ultrasonography, body measurements, and selected metabolic laboratory parameters will be assessed before the program and after six months.

Descripción general del estudio

Estado

Reclutamiento

Descripción detallada

This prospective single-arm interventional study will evaluate the effect of a structured six-month lifestyle-modification program on penile hemodynamic parameters and erectile function in adult men with metabolic syndrome-associated erectile dysfunction.

Participants will undergo baseline assessment including demographic and clinical data collection, anthropometric measurements, blood-pressure assessment, erectile-function evaluation using the International Index of Erectile Function-5, selected laboratory investigations, and penile duplex Doppler ultrasonography after intracavernosal administration of a vasoactive agent according to the local institutional protocol.

The lifestyle program will include individualized dietary counseling, recommendations for regular moderate-intensity aerobic physical activity, weight-reduction advice, smoking-cessation counseling for smokers, sleep-hygiene counseling, reduction of sedentary behavior, and behavioral reinforcement during follow-up visits. Participants will be followed monthly for adherence reinforcement and will undergo repeat clinical, laboratory, erectile-function, and penile hemodynamic assessments at six months.

The principal hypothesis is that structured lifestyle modification will improve penile hemodynamic parameters, particularly peak systolic velocity, and will improve erectile-function scores in men with metabolic syndrome-associated erectile dysfunction.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

55

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

      • Cairo, Egipto, 11633
        • Reclutamiento
        • Al-Hussein University Hospital, Al-Azhar University, Urology Department
        • Contacto:
      • Cairo, Egipto
        • Reclutamiento
        • Department of Urology, Al-Hussein and Sayed Galal University Hospitals, Al-Azhar University
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • Men aged 30-65 years.
  • Erectile dysfunction present for at least six months.
  • International Index of Erectile Function-5 score of 21 or less.
  • Metabolic syndrome diagnosed according to the International Diabetes Federation criteria.
  • Sexually active participants in a stable sexual relationship.
  • Willingness and ability to participate in the six-month lifestyle-modification program.
  • Ability to provide written informed consent.

Exclusion Criteria:

  • Erectile dysfunction primarily attributable to neurogenic, psychogenic, hormonal, or postsurgical causes.
  • Severe hypogonadism requiring immediate testosterone-replacement therapy.
  • Use of phosphodiesterase type 5 inhibitors, intracavernosal injections, vacuum erection devices, or other erectile-dysfunction treatment that cannot be discontinued before baseline assessment.
  • Significant penile anatomical abnormality that may interfere with penile duplex Doppler assessment, including Peyronie disease.
  • Previous pelvic surgery or pelvic radiotherapy likely to affect erectile function.
  • Severe or unstable cardiovascular disease that precludes sexual activity or participation in exercise-based lifestyle modification.
  • Uncontrolled diabetes mellitus, defined in the protocol as HbA1c greater than 10%.
  • Uncontrolled hypertension despite medical therapy.
  • Severe renal or hepatic impairment.
  • Active malignancy or life expectancy of less than one year.
  • Major psychiatric illness, cognitive impairment, or inability to comply with study procedures or follow-up.
  • Inability or refusal to provide written informed consent.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Structured Lifestyle Modification
Participants will receive a structured six-month lifestyle-modification program consisting of dietary counseling, moderate-intensity physical-activity advice, weight-management counseling, smoking-cessation counseling when applicable, sleep-hygiene advice, reduction of sedentary behavior, and monthly behavioral reinforcement.
Participants will receive an initial standardized counseling session followed by written lifestyle instructions and repeated monthly reinforcement. The program will target improved diet quality, reduced caloric intake, increased moderate-intensity aerobic activity, weight reduction according to baseline body mass index and waist circumference, smoking cessation when applicable, improved sleep hygiene, and reduced sedentary behavior. Adherence will be assessed using participant self-report and follow-up review over six months.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in penile peak systolic velocity from baseline to six months
Periodo de tiempo: Baseline and six months after initiation of the lifestyle-modification program.
Change in peak systolic velocity measured in centimeters per second by penile duplex Doppler ultrasonography after intracavernosal vasoactive-agent administration, comparing the baseline value with the six-month post-intervention value.
Baseline and six months after initiation of the lifestyle-modification program.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in resistive index
Periodo de tiempo: Baseline and six months.
Change in penile resistive index calculated from penile duplex Doppler measurements.
Baseline and six months.
Change in body weight
Periodo de tiempo: Baseline and six months.
Change in body weight measured in kilograms.
Baseline and six months.
Change in waist circumference
Periodo de tiempo: Baseline and six months.
Change in waist circumference measured in centimeters using a standardized measurement method.
Baseline and six months.
Change in end-diastolic velocity
Periodo de tiempo: Baseline and six months.
Change in the total score of the International Index of Erectile Function-5 (IIEF-5) questionnaire from baseline to 6 months. The IIEF-5 total score ranges from 5 to 25, with higher scores indicating better erectile function and lower scores indicating greater erectile dysfunction.
Baseline and six months.
Change in International Index of Erectile Function-5 / Sexual Health Inventory
Periodo de tiempo: Baseline and six months
Change in total score from baseline to 6 months. Score range 5-25; higher scores indicate better erectile function.
Baseline and six months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Abul-fotouh Ahmed, MD, Al-Azhar University

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

13 de agosto de 2026

Finalización primaria (Estimado)

24 de julio de 2027

Finalización del estudio (Estimado)

24 de noviembre de 2027

Fechas de registro del estudio

Enviado por primera vez

6 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

6 de agosto de 2026

Publicado por primera vez (Actual)

11 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

14 de agosto de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

13 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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