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RecruitingNCT07783958Updated Aug 25, 2026

Male Sexual Function and Sexual Quality of Life in Polygamous Versus Monogamous Marriages

An observational study in Erectile Dysfunction and Sexual Dysfunction, sponsored by Al-Azhar University. Recruiting at 1 site in Egypt. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-25.

Sponsored by Al-Azhar University · Observational

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
1,820
Ages
18 Years and older
Sex
Male
01

Study summary

This web-based comparative cross-sectional survey will assess sexual function, sexual quality of life, psychological status, and marital satisfaction among Egyptian men in monogamous and polygamous marriages. Eligible participants will be married Egyptian men aged 18 years or older who provide electronic informed consent and complete an anonymous Arabic-language questionnaire. The primary outcome will be sexual function measured using the Sexual Health Inventory for Men (SHIM/IIEF-5). Secondary outcomes will include Sexual Quality of Life-Male (SQOL-M), Depression Anxiety Stress Scales-21 (DASS-21), marital satisfaction, and sociodemographic and clinical predictors of impaired sexual function. Data will be analyzed using descriptive, comparative, correlation, and multivariable regression methods.

Read the detailed description

Sexual function and sexual quality of life are influenced by biological, psychological, social, and relationship-related factors. Marital structure may be associated with differences in sexual function, sexual satisfaction, psychological distress, and quality of life; however, evidence among Egyptian men is limited.

This study will use an anonymous Arabic-language web-based questionnaire to compare married Egyptian men in monogamous and polygamous marriages. Participants will be recruited from different Egyptian governorates through online dissemination of the survey. Before completing the questionnaire, participants will review the study information sheet and provide electronic informed consent.

The questionnaire will collect sociodemographic, clinical, lifestyle, sexual, psychological, and relationship-related information. Sexual function will be assessed using the Arabic version of the Sexual Health Inventory for Men/Sexual Health Inventory for Men-5 (SHIM/IIEF-5). Sexual quality of life will be assessed using the Sexual Quality of Life-Male questionnaire. Depression, anxiety, and stress will be assessed using the Depression Anxiety Stress Scales-21. Marital satisfaction and relationship satisfaction will be assessed using predefined Likert-type questions.

The monogamous group will include men currently married to one wife. The polygamous group will include men currently married to two or more wives. Participants will be analyzed according to marital structure, and additional descriptive analyses may be performed according to the number of wives among polygamous participants.

The primary analysis will compare SHIM scores and the proportion of participants with impaired sexual function between the two marital groups. Secondary analyses will compare sexual quality of life, psychological status, marital satisfaction, and other clinical and sociodemographic variables. Multivariable regression models will be used to assess whether marital structure is independently associated with impaired sexual function or poor sexual quality of life after adjustment for relevant confounding factors.

02

Conditions studied

  • Erectile Dysfunction
  • Sexual Dysfunction
03

In context

Erectile Dysfunction

701 studies on the registry are indexed under Erectile Dysfunction; 125 are open to participants now.

This study's planned enrollment of 1,820 is above the median of 130 across 125 observational studies indexed under Erectile Dysfunction.

Browse Erectile Dysfunction studies →

Lead sponsor

Al-Azhar University is the lead sponsor of 531 studies on the registry; 172 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Sampling method
Non-probability sample

Study population

The study population will consist of Egyptian men aged 18 years or older who are currently married and living in Egypt or residing in different Egyptian governorates. Participants will be classified into two observational groups according to their existing marital structure: men married to one wife and men married to two or more wives. Participants will be recruited through an anonymous Arabic-language web-based questionnaire. The study team will not assign or modify marital status or any other exposure.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Egyptian males aged 18 years or older.
  • Currently married at the time of questionnaire completion.
  • Currently in either a monogamous marriage, defined as marriage to one wife, or a polygamous marriage, defined as marriage to two or more wives.
  • Able to read and understand Arabic.
  • Willing to complete the anonymous online questionnaire.
  • Able to provide electronic before accessing the questionnaire

Exclusion criteria

Exclusion Criteria:

  • Unmarried, divorced, or widowed individuals.
  • Individuals who do not provide electronic .
  • Incomplete questionnaire responses that do not contain the primary outcome measure.
  • Duplicate or clearly invalid questionnaire responses.
  • Self-reported major psychiatric illness or neurological disease that substantially affects sexual function.
  • Participants receiving active treatment that substantially affects sexual function, unless the treatment can be documented and appropriately considered in the statistical analysis.
  • Individuals unable to read or understand Arabic.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
1,820 participants (estimated)
Patient registry
No

Groups and cohorts

  • Monogamous marriage

    Egyptian men aged 18 years or older who are currently married to one wife and complete the anonymous online questionnaire.

    Other: Monogamous marital structure

  • Polygamous marriage

    Egyptian men aged 18 years or older who are currently married to two or more wives and complete the anonymous online questionnaire.

    Other: Polygamous marital structure

Interventions

  • OtherMonogamous marital structure

    Existing marital structure consisting of one current wife at the time of questionnaire completion. This is an observational exposure and is not assigned, modified, or administered by the study team. Participants in this exposure group will complete the same anonymous Arabic-language questionnaire as participants in the polygamous-marriage group.

  • OtherPolygamous marital structure

    Existing marital structure consisting of two or more current wives at the time of questionnaire completion. This is an observational exposure and is not assigned, modified, or administered by the study team. Participants in this exposure group will complete the same anonymous Arabic-language questionnaire as participants in the monogamous-marriage group.

06

What researchers measure

Primary outcomes

  1. Sexual function score measured by the Sexual Health Inventory for Men

    Sexual function will be assessed using the five-item Sexual Health Inventory for Men, also known as the International Index of Erectile Function-5 (SHIM/IIEF-5). Scores range from 5 to 25, with higher scores indicating better erectile function. The mean or median SHIM score will be compared between men in monogamous and polygamous marriages.

    Time frame: Baseline (single assessment at questionnaire completion)

Secondary outcomes

  1. Proportion of participants with impaired sexual function

    Impaired sexual function will be defined as a SHIM/IIEF-5 score of 21 or less. The outcome will be reported as the number and percentage of participants with impaired sexual function in each marital-structure group.

    Time frame: Baseline (single assessment at questionnaire completion)

  2. Sexual Quality of Life-Male questionnaire score

    Sexual quality of life will be assessed using the Sexual Quality of Life-Male questionnaire. The total score will be reported according to the scoring system of the validated questionnaire, with higher scores indicating better sexual quality of life if applicable to the selected version. Scores will be compared between monogamous and polygamous marriage groups.

    Time frame: Baseline (single assessment at questionnaire completion)

  3. Relationship satisfaction score

    Relationship satisfaction will be assessed using predefined Likert-type questions regarding satisfaction with the marital relationship. Scores will be summarized and compared between monogamous and polygamous marriage groups, with higher scores indicating greater satisfaction.

    Time frame: Baseline (single assessment at questionnaire completion)

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 25, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07783958
Responsible party
Abul-fotouh Ahmed (Professor of Urology, Al-Azhar University) — Principal investigator
First posted
Aug 25, 2026
Start date
Aug 20, 2026
Primary completion
May 2027 (estimated)
Completion
Aug 2027 (estimated)
Last update
Aug 25, 2026

Study contacts

Abul-fotouh Ahmed, MD
Contact
abulfotouhahmed@yahoo.com
+201001066756
Abul-fotouh Ahmed, MD
principal investigator · Department of Urology, Faculty of Medicine, Al-Azhar University, Cairo, Egypt

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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