Actively Recruiting

Phase Not Applicable
Age: 35Years - 45Years
MALE
ID06716125

Lifestyle Changes in Obese Males With Sexual Dysfunction and Tinnitus

Led by Cairo University · Updated on 2024-12-04

40

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research focuses on obese males aged 35 to 45 who experience subjective tinnitus affecting both ears and sexual dysfunction, specifically erectile dysfunction lasting at least 24 weeks. The study aims to explore how lifestyle changes might influence these conditions by comparing different interventions. It is an interventional trial sponsored by Cairo University. Participants are randomly assigned into two groups, each with 20 males. Both groups follow a low-calorie diet for 12 weeks. Additionally, one group receives supervised aerobic treadmill walking for 45 minutes, three times a week, during the same 12-week period. This design evaluates the combined effect of diet and exercise versus diet alone. Throughout the 12 weeks, researchers will assess erectile function using the International Index of Erectile Function. They will also measure body mass index, waist circumference, tinnitus severity and discomfort via visual scales, the tinnitus handicap inventory, and blood markers such as triglycerides, high-density lipoprotein, and the atherogenic index. These assessments provide a comprehensive view of how the interventions impact sexual function, tinnitus, and metabolic health.

CONDITIONS

Brief Title

Lifestyle Changes in Obese Males With Sexual Dysfunction and Tinnitus

Who Can Participate

Age: 35Years - 45Years
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Obese males
  • Body mass index between 30 and 40 kg/m2
  • Males with bilateral subjective tinnitus lasting at least 24 weeks
  • Males with erectile dysfunction lasting at least 24 weeks
Not Eligible

You will not qualify if you...

  • Males with heart disease
  • Males with respiratory disease
  • Males with liver, musculoskeletal, or hepatic diseases
  • Males with diabetes

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 12 weeks

Participants follow a low calorie diet for 12 weeks. Participants in one group additionally perform supervised aerobic treadmill walking for 45 minutes, 3 times per week for 12 weeks.

Weekly visits for up to 12 weeks

Trial Site Locations

Total: 1 location

1

faculty of physical therapy Cairo university

Dokki, Giza Governorate, Egypt, 11432

Actively Recruiting

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Research Team

A

Ali Isamil, Lecturer

A

ahmed elfahl, Lecturer

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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