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The effect of sexual self-care education on sexual health and marital satisfaction of women with HIV-infected partners.

"Determining the Effect of a Sexual Self-Care Education Intervention on Sexual Health and Marital Satisfaction of Healthy Women with HIV-Positive Husbands: A Randomized Controlled Clinical Trial"

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170513033951N2
Enrollment
80
Registered
2025-06-02
Start date
2025-05-31
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sexual health and marital satisfaction of healthy women with HIV-positive partners.

Interventions

Intervention group: This study will be conducted as a randomized clinical trial with two experimental and control groups, after the necessary preparations, including approval by the Ethics Committee o

Sponsors

Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 49 Years

Inclusion criteria

Inclusion criteria: Being a woman and having an HIV-positive spouse (confirmed by medical documents or medical records) Negative HIV test result in the woman (woman is HIV negative = incompatible couple) Women of reproductive age 18 to 49 years Having lived together with your current spouse for at least 6 months Ability to read and write Having sexual activity Informed consent to participate in the study Absence of psychiatric illnesses or cognitive disorders (based on self-report) Not using psychotropic or narcotic drugs Not pregnant at the time of intervention No participation in similar interventions within the past 6 months

Exclusion criteria

Exclusion criteria: HIV infection in women during the study period Unwillingness to continue cooperation at any stage of the study Individuals not attending more than three sessions of the intervention program The occurrence of severe family or personal crises that disrupt the individual's participation process The woman became pregnant during the study Change in marital status during the study (divorce) Use of medications or treatments that have a serious impact on sexual or psychological functioning during the implementation of the intervention Development of a previously undiagnosed psychiatric or cognitive disorder during the study

Design outcomes

Primary

MeasureTime frame
Sexual health score. Timepoint: At the beginning of the study (before the intervention), at the end of the intervention, and 4 weeks after the intervention. Method of measurement: Sexual Self-Care Questionnaire for Women of Reproductive Age (FSHS): Female Sexual Health Self-care.;Marital satisfaction score. Timepoint: At the beginning of the study (before the intervention), at the end of the intervention, and 4 weeks after the intervention. Method of measurement: ENRICH Marital Satisfaction Questionnaire: Evaluation and Nurturing Relationship Issues, Communication and Happiness.

Secondary

MeasureTime frame
Sexual health score. Timepoint: At the beginning of the study (before the intervention), at the end of the intervention, and 4 weeks after the intervention. Method of measurement: Sexual Self-Care Questionnaire for Women of Reproductive Age (FSHS): Female Sexual Health Self-care.;Marital satisfaction score. Timepoint: At the beginning of the study (before the intervention), at the end of the intervention, and 4 weeks after the intervention. Method of measurement: ENRICH Marital Satisfaction Questionnaire: Evaluation and Nurturing Relationship Issues, Communication and Happiness.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohadese Motaharinezhad

Shahroud University of Medical Sciences

Motahari.m11@gmail.com+98 23 3239 5054

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026