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Effects of Early Abuse on Adult Intimate Relationships

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Completed

Conditions

Major Depressive Disorder
Post-traumatic Stress Disorder
Female Orgasmic Disorder
Female Sexual Arousal Disorder
Hypoactive Sexual Desire Disorder

Treatments

Behavioral: Expressive writing

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01803802
1R01HD051676
R01HD051676 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This study is designed to help us better understand the factors that affect the sexual lives of women who have been sexually mistreated during childhood. With this study we hope to learn about factors that may be promising targets for future treatments of sexual problems related to past sexual experiences. The investigators hypothesize that women who have experienced early sexual abuse are more likely to have sexual problems in adulthood than women who were not abuse in childhood.

Enrollment

148 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • at least one involuntary sexual experience, defined as "unwanted oral, anal, or vaginal intercourse, penetration of the vagina or anus using objects or digits, or genital touching or fondling," before age 16 and no less than 2 years prior to enrollment.
  • currently sexually active or cohabiting in a potentially sexual relationship.
  • current sexual dysfunction, distress, or low sexual satisfaction

Exclusion criteria

  • traumatic event in the previous three months
  • sexual abuse in the past two years
  • diagnosis of a psychotic disorder in the previous six months
  • significant suicidal or homicidal intent
  • currently receiving psychotherapy for sexual or abuse-related concerns
  • use of illicit drugs
  • in a currently abusive relationship

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Triple Blind

148 participants in 3 patient groups, including a placebo group

Time management
Placebo Comparator group
Description:
Writing prompts oriented towards objective recounting of previous day
Treatment:
Behavioral: Expressive writing
Sexual schema writing
Experimental group
Description:
Expressive writing prompts oriented towards beliefs about sexuality
Treatment:
Behavioral: Expressive writing
Trauma writing
Active Comparator group
Description:
Expressive writing prompts oriented towards processing traumatic experiences
Treatment:
Behavioral: Expressive writing

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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