Motivating HIV+ Women: Risk Reduction and ART Adherence (KHARMA)
This study has been completed.
Sponsor:
Emory University
Information provided by:
Emory University
ClinicalTrials.gov Identifier:
NCT00253045
First received: November 14, 2005
Last updated: June 21, 2011
Last verified: November 2005
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Purpose
The purpose of this study is to determine if a group motivational interviewing based intervention will increase adherence to antiretroviral medications and use of risk reduction behaviors.
| Condition | Intervention |
|---|---|
|
HIV AIDS |
Behavioral: Motivational groups |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Supportive Care |
| Official Title: | Motivating HIV+ Women: Risk Reduction and ART Adherence |
Resource links provided by NLM:
Genetics Home Reference related topics:
complement factor I deficiency
MedlinePlus related topics:
HIV/AIDS
U.S. FDA Resources
Further study details as provided by Emory University:
Primary Outcome Measures:
- Adherence to antiretroviral therapy [ Time Frame: Baseline, 2 weeks, 3, 6, 9 months post intervention ] [ Designated as safety issue: No ]Self report questionnaires, Electronic drug monitoring caps (MEMS)
- Use of Risk Reduction Behaviors [ Time Frame: Baseline, 2 weeks, 3, 6, 9 months post intervention ] [ Designated as safety issue: No ]Questionnaires about risky sexual behaviors, and substance use behaviors
- Clinical indicators [ Time Frame: Baseline, 2 weeks, 3, 6, 9 months post intervention ] [ Designated as safety issue: No ]CD4 and HIV viral load lab results from medical records
Secondary Outcome Measures:
- Self-Efficacy [ Time Frame: Baseline, Immediate post follow-up, 3, 6, 9 months post intervention ] [ Designated as safety issue: No ]
- Outcome Expectancy [ Time Frame: Baseline, 2 weeks, 3, 6, 9 months post intervention ] [ Designated as safety issue: No ]
- Personal Goals [ Time Frame: Immediate post follow-up, 3, 6, and 9 months post intervention ] [ Designated as safety issue: No ]
| Enrollment: | 207 |
| Study Start Date: | August 2004 |
| Study Completion Date: | January 2008 |
| Primary Completion Date: | January 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Motivational group
Group counseling using motivational interviewing
|
Behavioral: Motivational groups
Motivational interviewing in group format
|
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years to 85 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Infected with HIV
- Be on a new or different antiretroviral medication regimen or self report non-adherence to antiretroviral medications
- Must be 18 years of age or older
- Female by birth
- Understand and speak English
- Be willing to complete a screening interview to further determine if you are able to take part in the study
- Be willing to follow study requirements and use a MEMS cap on one of your antiretroviral meds
Exclusion Criteria:
- Under 18 years of age
- Transgender
- Males
- HIV negative
- Do not understand or speak English
- Do not achieve a satisfactory score on the screening interview
- Diagnosed as actively psychotic, severely depressed, or pose a risk of harm to themselves or others since these women may not be emotionally capable of sitting through lengthy, potentially emotional group or assessment sessions, or may be disruptive to other participants
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00253045
Locations
| United States, Georgia | |
| Nell Hodgson Woodruff School of Nursing, Emory University | |
| Atlanta, Georgia, United States, 30322 | |
Sponsors and Collaborators
Emory University
Investigators
| Principal Investigator: | Marcia McDonnell-Holstad, DSN,RN-C,FNP | Nell Hodgson Woodruff School of Nursing, Emory University |
| Study Director: | Bridget F. Jones, RN,MSN,BSEd | Nell Hodgson Woodruff School of Nursing, Emory University |
More Information
Publications:
| Responsible Party: | Marcia Holstad, Emory University |
| ClinicalTrials.gov Identifier: | NCT00253045 History of Changes |
| Other Study ID Numbers: | 1-RO1-NR008094-01A1 |
| Study First Received: | November 14, 2005 |
| Last Updated: | June 21, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Emory University:
|
Motivational Interviewing antiretroviral therapy medication adherence risk reduction behaviors |
women HIV AIDS |
Additional relevant MeSH terms:
|
Acquired Immunodeficiency Syndrome HIV Infections Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases |
Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Slow Virus Diseases Immunologic Deficiency Syndromes Immune System Diseases |
ClinicalTrials.gov processed this record on June 13, 2013