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Effectiveness of the Sexual Health Education Program on the Sexual Self Efficacy, Marital Adjustment and Intimacy

Effectiveness of the Sexual Health Education Program on the Sexual Self Efficacy, Marital Adjustment and Intimacy of Infertile Women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190203042601N1
Enrollment
60
Registered
2019-04-10
Start date
2019-03-30
Completion date
Unknown
Last updated
2019-04-23

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

Conditions

sexual self efficacy.

Interventions

Intervention 1: Intervention group:The intervention group will participate in a total of four two-hour group sessions of sex education and relaxation training will present in the form of lectures, Q&A

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: ? Conscious consent to enter the study ? Infertility women who did not want to treat infertility until two months later. ? Duration of infertility for more than 1 year ? The ability to read and write at least ? Have a lasting sexual activity (at least four weeks) Age of at least 20 and maximum 40 years ? The availability of the spouse ? Permanent marriage ? Consumers of drugs that cause sexual dysfunction, such as barbiturates, benzodiazepines (diazepam, oxazepam, chlordiazepoxide), antidepressants, antihypertensive drugs, etc.

Exclusion criteria

Exclusion criteria: ? Failure to participate in completing the questionnaire ? Failure to answer more than 10% of the questionnaire questions ? Having psychological support (participating in psychotherapy sessions, relaxation techniques, yoga, etc.) An experienced stressful event in the last three months (death or acute illness of close relatives, a major change in lifestyle)With the above criteria, 60 infertile women enter the study and will be randomly assigned to experimental and control groups.

Design outcomes

Primary

MeasureTime frame
Sexual Self Efficacy. Timepoint: Before the intervention and four weeks after its. Method of measurement: Sexual self-efficacy measurement tool is a standard self-efficacy questionnaire.;Marital Adjustment. Timepoint: Before the intervention and four weeks after its. Method of measurement: Marital adjustment will measure using Graham-bi spinner Marital Adaptation Inventory (DAS: Dyadic Adjustment Scale).;Marital Intimacy. Timepoint: Before the intervention and four weeks after its. Method of measurement: Marital intimacy will measure using Marital Intimacy Needs Questionnaire Bagarozzi (2001( (MINQ).

Secondary

MeasureTime frame
Sexual function. Timepoint: Before the intervention and four weeks after its. Method of measurement: Iranian Version of the Female Sexual Function Inventory (IV-FSFI).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Banaha

Babol University of Medical Sciences

sara.banaha20@yahoo.com+98 21 2247 3446

Outcome results

None listed

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