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The efficacy of Tele-based sexuality councelling on sextual function and sextual distress of primiparous women with exclusive breastfeeding and their spouses

The efficacy of Tele-based sexuality councelling on sextual function and sextual distress of primiparous women with exclusive breastfeeding and their spouses

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220424054637N2
Enrollment
140
Registered
2022-10-18
Start date
2022-10-23
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Sextual function , Sextual distress.

Interventions

Intervention 1: Intervention group: Before the intervention, the questionnaire link will be sent through the "Whatsapp "application and the people will be coded. In addition to routine postpartum car

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Primiparity Living with a spouse Have exclusive breastfeeding Have a singleton full-term birth (after 38 weeks) Being in the first six months after delivery Being accessible within the next two months Have a healthy child without physical problems or special diseases Have smartphone

Exclusion criteria

Exclusion criteria: Lack of sexual activity with spouse during the postpartum period Severe marital conflicts and the occurrence of unfortunate events (death of loved ones, accidents, etc.), Having a history of chronic mental and physical illness (check the records in the file and history)

Design outcomes

Primary

MeasureTime frame
Sextual function score. Timepoint: Before and immediately after the end of the study, one week, one month and two months after the intervention. Method of measurement: Female Sexual function Index FSFI-6,International index of erectile function: (IIEF-5).

Secondary

MeasureTime frame
The level of sexual distress of couples. Timepoint: Before and immediately after the end of the study, one week, one month and two months after the intervention. Method of measurement: Female Sexual Distress Scale (FSDS_R ).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Heydari

Qazvin University of Medical Sciences

mahhaid1371@gmail.com+98 86 4241 4105

Outcome results

None listed

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