Childhood Sexual Abuse, Vaginismus and Labor Dystocia

Depression Clinical Trial

— CSA-V-LD  

Official title:

Childhood Sexual Abuse, Vaginismus and Labor Dystocia: Towards a Theoretical Model

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT01530113
• Other study ID #: -0085-11
• Status: Not yet recruiting
• Phase: N/A
• First received: January 25, 2012
• Last updated: February 8, 2012
• Start date: March 2012
• Est. completion date: March 2015

Study information

• Verified date: January 2012
• Source: Hillel Yaffe Medical Center
• Contact: Mordechai Hallak, M.D, Prof.
• Phone: 972-4-6304244
• Email: mottih[@]hy.health.gov.il
• Is FDA regulated: No
• Health authority: Israel: Ethics Commission
• Study type: Observational

Clinical Trial Summary

The study aims to develop a theoretical model explicating the inter-relationships between Childhood Sexual Abuse (CSA), Partial Vaginismus (PV) and Labor Dystocia (LD), including their associations with Depression (D) as a mediating variable.

The following research hypotheses will be tested:

1. CSA will serve as a risk factor for D, PV and LD.

• pregnant women with a history of CSA will have higher levels of D compared to pregnant women without a history of CSA.

• pregnant women with a history of CSA will have more PV compared to pregnant women without a history of CSA.

• pregnant women with a history of CSA will have higher levels of LD compared to pregnant women without a history of CSA.

2. D will serve as a mediator between prenatal PV and LD.

3. PV will serve as a risk factor for LD.

4. postpartum PV will be affected by childbirth (LD vs. no LD) contingent on the level of D.

Description:

Previous studies indicate that childhood sexual abuse has long term implications to women's psychological and physical well-being; among them, depression, a plethora of gynecological symptoms and labor dystocia. Literature in the field also suggests that childhood sexual abuse may be a contributing factor to total and/or partial vaginismus: psycho-sexual disorders associated with significant difficulty and pain during attempted penetration, pelvic examinations and/or sexual relations.

The proposed quantitative longitudinal study aims to develop a theoretical model explicating the relationships between: childhood sexual abuse, prenatal and postpartum partial vaginismus, and childbirth (labor dystocia versus no labor dystocia); including their associations with depression as a mediating variable. Questionnaire responses of pregnant women (Hebrew/Arabic speakers) from the Hillel-Yaffe medical center in Israel will be included in the study.

Data collection will be extended across three time periods: prenatal (third trimester of pregnancy), within one month postpartum, and approximately six months postpartum. Study questionnaires will probe participant's socio-demographic and gynecological history, traumatic life events, sexual experiences, level of depression, partial vaginismus and sexual distress and the objective and subjective severity of their childbirth experience.

Simulations for this project were carried out to help set statistical significance goals and to determine the sample size needed to achieve these goals. From these simulations, a sample size of N=2000 was determined to be adequate and cost effective, to determine standard deviations SD (defining confidence interval ±SD) of about 0.022 for the correlations.

The potential significance of the study is twofold: Theoretically, the study represents a first of its kind effort to explore the relationships between child sexual abuse, prenatal and postpartum partial vaginismus, childbirth and depression, in a single comprehensive longitudinal research study. Practically, the study may potentially assist a wide range of health care professionals by:

1. providing a developing theory for evidence-based practice.

2. showing the need for integration of women's past history into prenatal and postnatal care as a means of lowering the risk for a traumatic birth experience and later psychological distress.

3. aiding in the development of intervention models for the treatment of women with a history of child sexual abuse and/or vaginismus during pregnancy and childbirth.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 2000
• Est. completion date: March 2015
• Est. primary completion date: March 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• pregnant women in their third trimester

Exclusion Criteria:

• alcohol addiction

• drug addiction

• mental retardation

• active psychopathology

Study Design

N/A

Related Conditions & MeSH terms

• Child Abuse
• Depression
• Dystocia
• Vaginismus

Locations

Country	Name	City	State
Israel	Department of Obstetrics and Gynecology, Hillel-Yaffe Medical Center	Hadera

Sponsors (2)

Lead Sponsor	Collaborator
Hillel Yaffe Medical Center	The Baruch Padeh Medical Center, Poriya

Country where clinical trial is conducted

Israel,