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Investigate the effectiveness of performing educational package based on consultant midwife on sexual function in postmenopausal women and sexual satisfaction of middle-aged couples

Investigate the effectiveness of performing educational package based on consultant midwife on sexual function in postmenopausal women and sexual satisfaction of middle-aged couples

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016112631117N1
Enrollment
100
Registered
2016-12-16
Start date
2016-11-07
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

Menopause. Primary ovarian failure

Interventions

Intervention 1: Control group: This group during the study will not be any intervention, but to consider the ethical aspects, after doing research, training manual containing the contents of the meeti
Behavior
Control group: This group during the study will not be any intervention, but to consider the ethical aspects, after doing research, training manual containing the contents of the meetings will be pres
Intervention group: Sessions will be established to a single couple. Educational – consultative sessions will be established four sixty-minute sessions once a week. The contents of the meeting include

Sponsors

Vice chancellor for research, Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
44 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: A written consent to participate in the study; Their husbands alive and living with his wife; One year from the last menstrual period of the past; They have a natural menopause; Obtaining a score less than 26/5 of the scale of sexual function; Having basic literacy; Having age between 44 to 55 years; Having sexual dysfunction, at least in the last 4 weeks; Lack of drug addiction; No diagnosis of severe physical or mental disease in postmenopausal women, according to GHQ questionnaire. Exclusion criteria: The receipt of any psychological or additional treatment such as hormone therapy for menopause before or during the study; Chronic diseases such as advanced physical and mental diabetes, multiple sclerosis, heart disease and psychosis; The occurrence of any event or crisis in their life such special events as the death of relatives, incurable disease in family members in the last month; receive any formal education about sex before or during the study; The absence of the wife of training sessions and Consultancy; Diagnosis of impotence in the IIEF questionnaire wife.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sexual function in postmenopausal women. Timepoint: A week before, two weeks after the last sessions, two months after the last sessions. Method of measurement: Female Sexual Function Questionnaire Rosen.

Secondary

MeasureTime frame
Sexual satisfaction of middle-aged couples. Timepoint: A week before, two weeks after the last sessions, two months after the last sessions. Method of measurement: International sexual satisfaction questionnaire Larson.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Khani Soghra

Mazandaran University Of Medical Sciences

s.khani@mazums.ac.ir khanisog343@gmail.com+98 11 3336 8918

Outcome results

None listed

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