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The Effectiveness of Consultation Based on PLISSIT model On sexual function of women during First six month after delivery

The Effectiveness of Consultation Based on PLISSIT model On sexual function of women during First six month after delivery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015062522921N1
Enrollment
90
Registered
2015-11-06
Start date
2015-11-01
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 problem. Sexual dysfunction,not caused by organic disorder or disease

Interventions

Intervention 1: just Routine consultation is done in control group. Intervention 2: In the interventional group, a meeting is done in an hour
that will talk about the problems of the patient and her sexual function although it may be opposite of therapist’s beliefs. In the next step the therapist gives a brief information about patient’s wo
Specific suggestions will be presented at the next step of the patient to enable her to manage her sexual problems. finally focused consultation is done by team psychiatrist.
Early detection
just Routine consultation is done in control group.
In the interventional group, a meeting is done in an hour

Sponsors

Vice chancellor for research and Technology? Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 39 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: primiparous and lactating women after a term singleton delivery? during 6 months after delivery? having at least one sexual problem (FSFI score<28? lack of stressful events during pregnancy and after childbirth? lack of complications in pregnancy and after childbirth? lack of mental and chronic physical illness. Exclusion criteria: becomes pregnant? lack of access to participation? the loss of the baby? away from his wife.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sexual Function. Timepoint: Before intervention; 4 weeks after intervention. Method of measurement: FSFI Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMojdeh Banaei

Shahid Beheshti University of Medical Sciences

Mojdeh.Banaei@Gmail.com ? Banaei.M@sbmu.ac.ir+98 21 2243 9888

Outcome results

None listed

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