Toward Gender Aware VA Healthcare: Development and Evaluation of an Intervention

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Department of Veterans Affairs
ClinicalTrials.gov Identifier:
NCT00156663
First received: August 25, 2005
Last updated: April 18, 2013
Last verified: February 2007

August 25, 2005
April 18, 2013
May 2004
Not Provided
Gender Awareness is measured during the pre-test, immediately after the educational program, and approximately four weeks after the subject participates in the educational program. [ Designated as safety issue: No ]
Gender Awareness is measured during the pre-test, immediately after the educational program, and approximately four weeks after the subject participates in the educational program.
Complete list of historical versions of study NCT00156663 on ClinicalTrials.gov Archive Site
Participants rate their enjoyment of the educational program and offer recommendations for the program as needed. [ Designated as safety issue: No ]
Participants rate their enjoyment of the educational program and offer recommendations for the program as needed.
Not Provided
Not Provided
 
Toward Gender Aware VA Healthcare: Development and Evaluation of an Intervention
Toward Gender Aware VA Health Care: Development and Evaluation of an Intervention

The purpose of this study was to develop and evaluate an educational program intended to raise staff awareness about women veterans and their health care needs and preferences.

OBJECTIVES:

The primary objective of this project was to develop and evaluate a computerized program that would enhance Veterans Health Administration (VHA) employees� awareness of women veterans and their health-care needs. The program was designed to challenge negative stereotypes about female patients (gender-role ideology), increase empathy toward female patients� needs (gender sensitivity), and enhance knowledge regarding women veterans and aspects of their VHA care (knowledge).

DESIGN/METHODS:

Phases I involved generating content for the computerized interactive program. Phase II involved creating the 30-minute program. The Phase III evaluation of the program involved a two-group pretest�posttest�follow-up equivalent control group design at two facilities with a third facility comparison group. At the first two facilities, employees who provide either direct or ancillary care to patients were randomly assigned to either the treatment or the control group. Participants in the treatment group completed the program entitled Caring for Women Veterans. Participants in the control group and those at the third site completed a 30-minute program entitled Managing Stress. The data from the third site were included to test for infusion of the treatment effect within same-site groups. Gender awareness was evaluated at three time points using the Gender Awareness Inventory-VA (GAI-VA). Participants completed the GAI-VA several weeks prior to completing the computerized program (Time 1, n =339), immediately after completing the program (Time 2, n = 249), and approximately one month after the program (Time 3, n = 167). Participants also completed a qualitative evaluation of the program at Time 2.

STATUS:

Complete.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Women's Health
Behavioral: Caring for Women Veterans
Arm 1
Intervention: Behavioral: Caring for Women Veterans
Vogt DS, Barry AA, King LA. Toward gender-aware health care: evaluation of an intervention to enhance care for female patients in the VA setting. J Health Psychol. 2008 Jul;13(5):624-38.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
250
September 2005
Not Provided

Inclusion Criteria:

Participants must be VHA employees who have direct or indirect contact with patients.

Exclusion Criteria:

Employees who have no contact with patients.

Both
18 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00156663
GEN 20-057
No
Department of Veterans Affairs
Department of Veterans Affairs
Not Provided
Principal Investigator: Dawne S Vogt, PhD BA VA Boston Health Care System, Jamaica Plain
Principal Investigator: Lynda A. King, PhD VA Boston Health Care System
Department of Veterans Affairs
February 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP