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The effectiveness of consuling with EXPLISSIT approach on sexual function and marital satisfaction in newly delivered women

The effectiveness of consuling with EXPLISSIT approach on sexual function and marital satisfaction in newly delivered women: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20111122008170N12
Enrollment
68
Registered
2018-05-02
Start date
2018-06-05
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Sexual dysfunction in women newly delivered. Unspecified sexual dysfunction, not caused by organic disorder or disease

Interventions

Intervention 1: Intervention group: In the intervention group, sexual counseling will be given by the trained midwife during a 60-90 minute or more session in accordance with the EXPLISSIT model and w

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Having at least a literacy guide according to the person herself Score less than 28 from the Female Sexual Function Index questionnaire (FSFI ) Single lactating women Being between 3 and 6 months after childbirth Having a call number to follow up Husband's monogamous

Exclusion criteria

Exclusion criteria: Exposure to a stressful event or any complication of pregnancy during pregnancy and postpartum (for example: death of a family members) according to the person herself Having a history of depression pre-pregnancy, during pregnancy and postpartum according to the person herself Having a history of chronic physical and mental illness such as cardiovascular disease, diabetes, severe depression and high blood pressure that consumes the drug according to the person herself Use of any effective medicines on person's sexual response, (antihypertensive drugs, thiazide diuretics, antidepressants, antihistamines, Barbiturates, narcotics, diazepins, amphetamines and cocaine) according to the person herself Child with known anomalies or preterm (less than 37 weeks) Marriage separation (emotional divorce or full divorce) The death of the baby after delivery for any cause Addiction to a person or his wife according to the person herself The history of sexual dysfunction before pregnancy in couples (including disorders of sexual desire or orgasm in women, early and late ejaculation, erectile dysfunction and male orgasm) according to the person herself

Design outcomes

Primary

MeasureTime frame
Sexual function score. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Female Sexual Function Index questionnaire.;Marital satisfaction score. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Enrich Marital Satisfaction questionnaire.

Secondary

MeasureTime frame
Quality of sexual life score. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Female sexual quality of life questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRobab Gholizadeh

Tabriz University of Medical Sciences

205rgh@gmail.com+98 45 3324 8888

Outcome results

None listed

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