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A Mindfulness-based Intervention for Older Women With Low Sexual Desire

University of Pittsburgh logo

University of Pittsburgh

Status

Completed

Conditions

Female Sexual Dysfunction
Sexual Dysfunction
Hypoactive Sexual Desire Disorder

Treatments

Behavioral: mindfulness-based multicomponent intervention
Behavioral: general health education group

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03232801
PRO15060240
K23AG052628 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The overall aim of this research is to adapt and pilot test a multi-component, mindfulness-based behavioral intervention for women age 50 and older with low sexual desire.

Full description

Specifically, the investigators will conduct a pilot randomized controlled trial to assess the feasibility, acceptability, and preliminary efficacy of the intervention. Fifty women will be randomized to the mindfulness intervention or an educational control group. Both groups will be conducted in 3 sessions over 6 weeks in groups of 10 women. Feasibility, acceptability, facilitators, and barriers will be assessed by surveys after each session and after intervention completion. Preliminary efficacy will be assessed by measures of sexual desire, sexual function, and overall sexual satisfaction at 6 and 12 weeks.

Enrollment

62 patients

Sex

Female

Ages

50+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • meet criteria for a diagnosis of Female Sexual Interest/Arousal Disorder
  • English-speaking
  • have a current sexual partner with whom they are or would like to be sexually active

Exclusion criteria

  • active major depression
  • active substance abuse
  • current intimate partner violence
  • partner with active major depression
  • partner with active major substance abuse
  • significant relationship dissatisfaction
  • current use of antidepressants
  • untreated dyspareunia (sexual pain)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

62 participants in 2 patient groups

mindfulness group
Experimental group
Description:
A multicomponent group-based intervention rooted in mindfulness, administered in 3 sessions over 6 weeks
Treatment:
Behavioral: mindfulness-based multicomponent intervention
educational group
Active Comparator group
Description:
A general midlife health and aging educational group, administered in 3 sessions over 6 weeks
Treatment:
Behavioral: general health education group

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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