The effect of consultation versus no consultation on sexual function of lactating women with decreased libido

The effect of consultation versus no consultation on sexual function of lactating women with decreased libido: a randomized clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120215009014N247

Enrollment

104

Registered

2018-10-27

Start date

2018-11-16

Completion date

Unknown

Last updated

2019-01-14

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

Conditions

Decreased libido. Decreased libido

Interventions

Intervention 1: Intervention group: Routine pregnancy care and a face-to-face consultation one hour a week for 4 weeks. Intervention 2: Control group: Just pregnancy care.

Eligibility

Sex/Gender

Female

Age

18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Age of 18 to 35 years; Lactating women; Decreased libido; Term singleton labor; Exclusive breastfeeding; Living with husband; Ability to speech Persian; Literate

Exclusion criteria

Exclusion criteria: Pregnancy; Stressful accidents; Pregnancy complications; Mental or physical disease; Using opioid or alcohol; Death or disease of the newborn

Design outcomes

Primary

Measure	Time frame
Assessing sexual function. Timepoint: Before intervention and 4 weeks after that. Method of measurement: Using a standard questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTahereh Heshmatian

Hamedan University of Medical Sciences

tara.hekmat@gmail.com+98 81 3838 0572

Outcome results

None listed

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