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The effect of cognitive behavioral counseling and Extended Permission; Limited information; Specific Suggestion; Referral for intensive therapy (EX PLISSIT) model on sexual function and sexual satisfaction in women during lactation

Compare the effectiveness of Midwifery counseling based on cognitive behavioral counseling approach and conseling based on Extended Permission;Limited information; Specific Suggestion; Referral for intensive therapy( EX PLISSIT) model on sexual function and sexual satisfaction in women during lactation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016040827280N1
Enrollment
102
Registered
2016-06-18
Start date
2016-05-21
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 function and satisfacation of lactation period. Lack or loss of sexual desire

Interventions

Intervention 1: Intervention2:3 sessions counseling based on EX PLISSIT. Intervention 2: Intervention group1: 4 group sessions based on cognitive behavioral counseling for 1.5 hours. Intervention 3: c
Prevention
Intervention2:3 sessions counseling based on EX PLISSIT.
Intervention group1: 4 group sessions based on cognitive behavioral counseling for 1.5 hours.
control group: Do not receive any intervention.

Sponsors

Vice Chancellor for research; Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: living on Neyshabur city; having at least primary education; life with spouse ; having sexual relation; maximum one year after of delivery; nulliparous ; breastfeeding; having psychosomatic healthy; Before entering the study has not been treated sexual problems. Exclusion criteria: happening the stressful event in the past month; taking drugs that affect sexual function; in the EX PLISSIT group if you need a referral; the referral is given and the excluded .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sexual function. Timepoint: Before; immediately and one month after intervention. Method of measurement: Female sexual function standard Questionnare.

Secondary

MeasureTime frame
Sexual satisfacation. Timepoint: Before; immediately and one month after intervention. Method of measurement: Larson sexual satisfacation standard questionnare.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahdieh Eshghi

Shahroud university of medical sciences

MAHD_MOHAMAD@YAHOO.COM+98 23 3239 7213

Outcome results

None listed

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