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Effectiveness of Counseling on Sexual Dysfunction of Women with Polycystic Ovarian Syndrome

Effectiveness of Sexual Counseling on Sexual Dysfunction of Women with Polycystic Ovarian Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201512023034N16
Enrollment
80
Registered
2017-04-14
Start date
2017-04-21
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

Sexual Dysfunction. Sexual dysfunction, not caused by organic disorder or disease

Interventions

Intervention 1: First, the Female sexual Function Index questionnaire (FSFI) will be completed by 80 patients with inclusion criteria in the presence of researcher, individually . Then randomely , p
Treatment - Drugs
First, the Female sexual Function Index questionnaire (FSFI) will be completed by 80 patients with inclusion criteria in the presence of researcher, individually . Then randomely , patients will be
At the end of intervention, training manual wich contains information about sexual responsive cycle, physiology and anatomy of the genital tract, polycystic ovarian syndrome and its side effects, etc

Sponsors

vice chancellor for Research, School of Nursing and Midwifery, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: Married; 18_45 years’ old; Iranian; Having at least degree of knowledge; Having sexual activity during past six months; The definitive diagnosis of the polycystic ovarian syndrome by a gynecologist and records in document which is based on the criteria of Rotterdam; Having sexual function score that is less than 28 before intervention; Lack of pregnancy and lactation and unwillingness to be pregnant during intervention; Lack of other acute physical and mental disease and endocrine disorder like thyroid disorders, diabetes based on the patient’s medical document; Lack of consumption alcohol and drugs by patients and her husband according to the patient’s reports; Lack of consumption drugs that are effective on sexual activity like ant depression, antihypertensive drugs...; Lack of consumption of any drugs or hormonal intervention during the last 60 days before intervention; Lack of history of women surgery such as genital surgery and breast surgery; Lack of sexual dysfunction by patient’s husband (according to patients reports); Lack of participation in training classes to counseling for sexual dysfunction; Lack of stressful events that are unrelated to pregnancy Exclusion criteria: Missing one of the session; Occurrences of stressful events that are unrelated to pregnancy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Arousal. Timepoint: Prior, immediatly and eight weeks after last session of counseling in working group and for control group, eight weeks after filling out the initial questionnaire. Method of measurement: Female Sexual Function Index questionnaire.;Lubrication. Timepoint: Prior, immediatly and eight weeks after last session of counseling in working group and for control group, eight weeks after filling out the initial questionnaire. Method of measurement: Female Sexual Function Index questionnaire.;Orgasm. Timepoint: Prior, immediatly and eight weeks after last session of counseling in working group and for control group, eight weeks after filling out the initial questionnaire. Method of measurement: Female Sexual Function Index questionnaire.;Desire. Timepoint: Prior, immediatly and eight weeks after last session of counseling in working group and for control group, eight weeks after filling out the initial questionnaire. Method of measurement: Female Sexual Function Index questionnaire.;Sexual Dysfunction. Timepoint: Prior, immediatly and eight weeks after last session of counseling in working group and for control group, eight weeks after filling out the initial questionnaire. Method of measurement: Female Sexual Function Index questionnaire.;Pain. Timepoint: Prior, immediatly and eight weeks after last session of counseling in working group and for control group, eight weeks after filling out the initial questionnaire. Method of measurement: Female Sexual Function Index questionnaire.;Satisfication. Timepoint: Prior, immediatly and eight weeks after last session of counseling in working group and for control group, eight weeks after filling out the initial questionnaire. Method of measurement: Female Sexual Function Index questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFahimeh Golbabaei

School Nursing and Midwifery, Iran University of Medical Sciences

farnaz2006_1000@yahoo.com+98 21 8888 2885

Outcome results

None listed

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