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

Sponsor
US Department of Veterans Affairs (U.S. Fed)
Overall Status
Completed
CT.gov ID
NCT00156663
Collaborator
(none)
250
2
1
16
125
7.8

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Caring for Women Veterans
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
250 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Official Title:
Toward Gender Aware VA Health Care: Development and Evaluation of an Intervention
Study Start Date :
May 1, 2004
Actual Study Completion Date :
Sep 1, 2005

Arms and Interventions

Arm Intervention/Treatment
Other: Arm 1

Behavioral: Caring for Women Veterans

Outcome Measures

Primary Outcome Measures

  1. 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. []

Secondary Outcome Measures

  1. Participants rate their enjoyment of the educational program and offer recommendations for the program as needed. []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

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

Exclusion Criteria:

Employees who have no contact with patients.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Edith Nourse Rogers Memorial Veterans Hospital, Bedford, MA Bedford Massachusetts United States 01730
2 VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA Boston Massachusetts United States 02130

Sponsors and Collaborators

  • US Department of Veterans Affairs

Investigators

  • Principal Investigator: Dawne S Vogt, PhD BA, VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA
  • Principal Investigator: Lynda A. King, PhD, VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
US Department of Veterans Affairs
ClinicalTrials.gov Identifier:
NCT00156663
Other Study ID Numbers:
  • GEN 20-057
First Posted:
Sep 12, 2005
Last Update Posted:
Apr 7, 2015
Last Verified:
Feb 1, 2007

Study Results

No Results Posted as of Apr 7, 2015