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A comparative study on the effect of face-to-face or group education during the pregnancy period and postpartum

A comparative study on the effect of face-to-face or group education during the pregnancy period and postpartum on sexual function of the couples

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014080518500N2
Enrollment
64
Registered
2015-07-06
Start date
2013-03-10
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 function. Unspecified sexual dysfunction, not caused by organic disorder or disease

Interventions

Intervention 1: Intervention "face-to-face education" In the face-to-face education group, education is conduct in a 90–120 min session through questions and answers and the education
Behavior
Intervention "face-to-face education" In the face-to-face education group, education is conduct in a 90–120 min session through questions and answers and the educational issues, dete
Intervention "group education" In the group education group, the subjects are divide into three 10-13 subject groups and the education is conduct similar to face-to-face education group durin

Sponsors

Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Iranian nationality; couples’ being a Muslim; gestational age of over 20 weeks; women’s age under 40 years and men’s age around 50 years; signing a written consent form by the couples to attend the study; no history of medical diseases in couples; no consumption of the medication contraindicating with sexual function; no addiction to drugs in any of the couples; no high risk pregnancy; and no experience of an acute stress during recent years such as a child’s death, spousal treason; acute disease etc in any of the couples, Exclusion criteria; postpartum depression; The use of vacuum or forceps delivery; birth trauma; weighing more than 4000 gr at birth; postpartum vaginal disorders; infant mortality.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sexual function. Timepoint: pre test, One month after the intervention and 10 weeks after delivery. Method of measurement: Female Sexual Function Index(FSFI) and Brief form of Sexual Function Inventory (BSFI).

Secondary

MeasureTime frame
A comparative study on the effect of face-to-face or group education. Timepoint: Before the intervention, after intervention, 10 weeks after delivery. Method of measurement: Female Sexual Function Index(FSFI) and Brief form of Sexual Function Inventory (BSFI).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Mohammadi Mahdiabadzade

Nursing and Midwifery Care Research Center, Faculty of Nursing and Midwifery, Isfahan University of

ba_zendegy@yahoo.com; maryammohamady@nm.mui.ac.ir+98 31 3681 6512

Outcome results

None listed

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