Consulting relationship to satisfaction and sexual function. Lack or loss of sexual desire
Conditions
Interventions
Intervention 1: In the interventional group, meetings once a week over 4 weeks is done in an hour
The first session will talk about the problems of the patient and her sexual function although it may be opposite of therapist’s beliefs. In the second session the therapist gives a brief information
Specific proposals will be presented at the third session of the patient to enable her to manage her sex problems. In the fourth session focused consultation is done by team psychiatrist. Intervention
Early detection
just Routine prenatal care is done in control group.
In the interventional group, meetings once a week over 4 weeks is done in an hour
Specific proposals will be presented at the third session of the patient to enable her to manage her sex problems. In the fourth session focused consultation is done by team psychiatrist.
Sponsors
Vice chancellor for Research and Technology, Hamedan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria include: The age range 18-35 years; single fetus and gestational age 24-26 weeks; lack of mental disorders according to psychiatrist ; not having gestational diabetes melitus, preeclampcia, bleeding, premature rupture of membranes; not taking sedative drugs; having sexual dysfunction confirmed by a psychiatrist; not having a history of having sexual dysfunction before pregnancy; exclusively female sexual dysfunction confirmed by psychiatrist. Exclusion criteria includes: occuring any problem in pregnancy during study (abruption, fetal abnormal situation, cord prolapse, bleeding, diabetes, hypertension, preterm labor); abnormal pattern of fetal heart rate or decrease of fetal movements that require medical intervention.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual satisfaction. Timepoint: Before intervention; 2 weeks after intervention; 4 weeks after intervention. Method of measurement: Lindaberg Questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Sextual function. Timepoint: Before intervention; 2 weeks after intervention; 4 weeks after intervention. Method of measurement: FSFI Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyedeh Zahra Masoumi
Hamedan University of Medical Sciences
Outcome results
None listed