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The effect of sexual counseling based on the sexual health model on sexual quality of life and sexual satisfaction among reproductive age women

The effect of counseling based on the sexual health model on sexual quality of life and sexual satisfaction among reproductive age women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251210068282N1
Enrollment
100
Registered
2026-02-23
Start date
2026-02-21
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Sexual Counselling. Counseling related to sexual attitude

Interventions

Intervention 1: Intervention group: Sexual health model. Counseling will be in three face-to-face sessions and the sessions will last 60-90 minutes. The content of the sessions will cover ten aspects
in the second session, (anatomy and sexual function), (body image), and (positive sexual desires)
and in the third session, (health care and safer sex), (fantasy), (challenges facing sexual health), and (spirituality). Intervention 2: Control group: The control group will also receive routine repr

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Ages between 15-49 years old Being married Being literate in reading and writing Being sexually active in the last month Not pregnant or breastfeeding Absence or history of known mental and physical illness that has a negative impact on sexual relations Not taking drugs to reduce sexual desire not use addictive substances and alcohol Lack of self-report of sexual dysfunction in the spouse No self-reported participation in any training courses on marital and sexual problems Not having extramarital relations of each couple

Exclusion criteria

Exclusion criteria: People who do not consent to participate in the study People who cannot attend counseling or follow-up sessions

Design outcomes

Primary

MeasureTime frame
Sexual Quality Of Life. Timepoint: Before, immediately and 4 weeks after the intervention. Method of measurement: Sexual Quality Of Life Questionnaire-Female.;Sexual satisfaction. Timepoint: Before, immediately and 4 weeks after the intervention. Method of measurement: Larson Sexual Satisfaction Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra ZamiriAraste

Hamedan University of Medical Sciences

zahrazamiriaraste1997@yahoo.com+98 81 3838 0572

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026