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effect of education on sexual function

Effect of educational package on the sexual function of cold-temper women in the reproductive age

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170623034717N1
Enrollment
80
Registered
2018-01-02
Start date
2017-11-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Other sexual disorders. Other sexual disorders

Interventions

Intervention 1: Specific training will be given, three weeks, twice a week, each session 60 minutes to the intervention group by lecture, question and answer and group discussion. Intervention 2: Cont
Lifestyle
Specific training will be given, three weeks, twice a week, each session 60 minutes to the intervention group by lecture, question and answer and group discussion
Control group: without training

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: female gender haviIranian cold-tempered womenng consent letter aged 18 to 40 Muslim the participants must be educated. living in Mashhad having sexual activity in the last 4 weeks Body mass index between 19.8_29 kg/m2 sexual function score (FSFI) <28 Tempered type determination score <14 The allocated groups are females whose scores in depression, anxiety and stress questionnaire are lesser than 14, 10 and 17, respectively

Exclusion criteria

Exclusion criteria: Taking medicine affecting sexual function happening stressful events during the past 6 months for any of couples being under psychiatric treatment for mental disorders having severe depression drug or alcohol addiction in any of couple No tendency to cooperate with research team having major conflicts with husband studying books or consulting about sexual issues during the past 6 months studying books or consulting about marital relations during the past 6 months being under treatment for sexual dysfunction in any of couple taking medicine lead to change in sexual desire during the past 3 months

Design outcomes

Primary

MeasureTime frame
Improve female sexual function. Timepoint: Before intervention, immediately after intervention. Method of measurement: Sexuality Questionnaire (FSFI).

Secondary

MeasureTime frame
Pain. Timepoint: 4 weeks after the end of the intervention. Method of measurement: Visual Analogue Scale (0 to 10).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNasim Baradaran Akbarzadeh

Mashhad University of Medical Sciences

baradarann941@mums.ac.ir+98 51 3760 6724

Outcome results

None listed

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