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The effect of counseling versus no counseling on sexual satisfaction in women with sexual desire disorder

The effect of counseling versus no counseling on sexual satisfaction in women with sexual desire disorder: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201607059014N106
Enrollment
120
Registered
2016-07-20
Start date
2016-07-22
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 desire disorder. Lack or loss of sexual desire

Interventions

Intervention 1: Routine treatment plus 7 counseling session twice a week 90 minutes each. Intervention 2: Just routine healthcare without counseling.
Treatment - Drugs
Routine treatment plus 7 counseling session twice a week 90 minutes each.
Just routine healthcare without counseling

Sponsors

Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 49 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: hypoactive sexual desire; age of18 to 49 years; the ability to read and write, at least one year has passed from marriage. Exclusion criteria: pregnancy or breastfeeding; having chronic disease; mental disorders; using OCP; non-continuous participation in training sessions.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Measuring hypoactive sexual desire. Timepoint: before intervention and one month later. Method of measurement: using questionnaire.;Measuring sexual satisfaction. Timepoint: before intervention and one month later. Method of measurement: using Hudson's questionnaire.

Secondary

MeasureTime frame
Nothing. Timepoint: Nothing. Method of measurement: Nothing.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBanafsheh Bojarzadeh

School of Nursing and Midwifery

b.bojar99@gmail.com+98 81 3838 1086

Outcome results

None listed

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