Qualitative Research on Women With Congenital Adrenal Hyperplasia

Completed

• Conditions: Congenital Adrenal Hyperplasia
• Interventions: Other: Interview

• Registration Number: NCT00559078
• Lead Sponsor: Lehigh University

Brief Summary

This qualitative interview-based study will investigate the impact that living with congenital adrenal hyperplasia has for women in the following areas: health-related quality of life (HRQL), psychological health, and health-seeking behaviors.

Detailed Description

Congenital Adrenal Hyperplasia is a chronic-illness requiring life-long treatment and is caused by an inherited enzyme deficiency that leads to an overproduction of hormones produced by the adrenal glands, which in turn, masculinizes the female genitalia before birth. While the mechanisms by which CAH influences physiological development are understood, the impact of this hormonal elevation on health-related quality of life (HRQL), psychological health, and health-seeking behaviors is less clear. This study is guided by three research questions: (1) how does CAH influence HRQL domains (physical, functional, emotional and interpersonally), (2) how does CAH influence the mental health of women diagnosed with CAH, and (3) how does CAH influence decisions to seek help from a counselor? Semi-structured qualitative interviews will be conducted with women with CAH. Interviews will be analyzed through the Consensual Qualitative Research (CQR) methodology.

Study Timeline

• Study Start: 2007-07
• Study First Submitted: 2007-11-15
• Study First Submitted QC: 2007-11-15
• Study First Posted: 2007-11-16
• Study Completion: 2009-05
• Status Verified: 2009-11
• Last Update Submitted: 2009-11-06
• Last Update Posted: 2009-11-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 16

Inclusion Criteria

• 46XX, Females
• Diagnosed by a physician with CAH (either simple-virilizing or salt-losing types)
• Willing to complete a brief demographic questionnaire and participate in an hour long telephone interview

Exclusion Criteria

• Non-classical or late-onset CAH

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
CAH	Interview	Women diagnosed with CAH (either simple virilizing or salt-losing)

Primary Outcome Measures

Name	Time	Method
Telephone interview consisting of approximately 7 open ended questions addressing domains of HRQL, Mental Health and Support	1 hour

Secondary Outcome Measures

Name	Time	Method
Demographic Questionnaire	15 minutes

Trial Locations

Locations (1)

Lehigh University; 🇺🇸 Bethlehem, Pennsylvania, United States