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Behavioral Activation/Armodafinil to Treat Fatigue in HIV/AIDS

Primary Purpose

Hiv, Fatigue, Goals

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Behavioral Activation Therapy
Supportive Counseling
Sponsored by
Research Foundation for Mental Hygiene, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hiv focused on measuring HIV+, fatigue, return to work

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • HIV+, ages 18-70
  • Under the care of a medical provider
  • Clinically significant fatigue
  • Speaks English
  • Able and willing to give informed consent
  • Patient seeks either work or vocational training but is blocked from doing so by current fatigue

Exclusion Criteria:

  • Primary care provider does not approve of study participation
  • Medical rule-outs such as anemia, hypothyroidism, hypogonadism or other condition that may account for fatigue
  • Abnormal EKG
  • Untreated major depressive disorder; psychosis, bipolar disorder
  • Current substance abuse/dependence
  • Clinically significant suicidal ideation

Sites / Locations

  • New York State Psychiatric Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Behavioral activation therapy

supportive counseling (SC)

Arm Description

The Behavioral Activation Program for Energy and Productivity (BA-PEP) is a manualized, 8-session intervention, scheduled to coincide with maintenance armodafinil treatment. It is a structured counseling program with homework, short-term activities and goals, and includes problem-solving, identification of barriers and strategies for their resolution, with an ongoing focus on achieving employment or training.

Supportive counseling is designed to create an empathic, accepting environment, to direct attention to the patient's feelings and to facilitate acceptance of affective experience using supportive statements, reflective listening and empathic communications.

Outcomes

Primary Outcome Measures

Employment or enrollment in vocational classes as measured by Goal Attainment Scaling
Goal Attainment Scaling assesses degree of success in reaching a pre-specified set of goals initially enumerated at study entry, with a 5-point score range. A score of zero is assigned to success in attaining the specified goal, with 2 greater and 2 lesser levels of accomplishment also specified.

Secondary Outcome Measures

Increased environmental interactions as measured by the EROS: Environmental Rewards Observation Scale.
This is a standardized 10-item scale with a 4-point agree/disagree response format.

Full Information

First Posted
July 7, 2010
Last Updated
December 19, 2016
Sponsor
Research Foundation for Mental Hygiene, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01158443
Brief Title
Behavioral Activation/Armodafinil to Treat Fatigue in HIV/AIDS
Official Title
Behavioral Activation/Armodafinil to Treat Fatigue in HIV/AIDS
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
March 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Research Foundation for Mental Hygiene, Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is an integrated medication/behavioral intervention program to increase energy, activity level and goal attainment in a sample of HIV+ adults whose presenting problems include both clinically significant fatigue and unmet vocational goals. Based on previous studies, the investigators found that many patients fail to achieve desired goals even though energy is restored by medication. To address this failure of goal attainment, the investigators will evaluate a behavioral intervention, originally based on Behavioral Activation Treatment for Depression, and modified as Behavioral Activation Program for Energy and Productivity or BA-PEP. The intervention will be conducted with patients who experience clinically significant fatigue and who want to work or receive work-related training (paid or volunteer, part time or full time) or education once energy improves with medication (armodafinil).
Detailed Description
The investigators propose an integrated medication/behavioral intervention program to increase energy, activity level and goal attainment in a sample of people with HIV/AIDS whose presenting problem is clinically significant fatigue and unmet vocational goals. Based on a recently completed randomized controlled trial (RCT) of modafinil and ongoing RCT of armodafinil, the investigators found that many patients fail to achieve desired goals even though energy is restored by medication. To address this failure of goal attainment, the team will develop and pilot a behavioral intervention, originally based on Behavioral Activation Treatment for Depression of Lejuez et al. and modified by Dr. Daughters as "Behavioral Activation Program for Energy and Productivity, or 'BA-PEP'". The intervention will be conducted with patients who experience significant fatigue, and who want to work or get work-related training or education once their energy improves with armodafinil treatment. It is intended for eventual implementation in HIV clinics and community agencies with work development programs. The intervention development includes both formative work and pilot studies. The formative work comprises in-depth patient interviews, focus groups with providers, a Project Advisory Board, and a separate Work Group. Their input will be used to modify their BA-PEP intervention to promote achievement of goals selected by each patient, once fatigue has been ameliorated with armodafinil, and to further adapt the attention control supportive counseling intervention. With this input, the investigators will conduct an exploratory study using BA-PEP with 12 patients responsive to armodafinil. After further modifications, investigators will conduct a feasibility trial with 30 armodafinil-responsive patients randomized 2:1 to BA-PEP or an attention control, supportive counseling. The main behavioral outcome is employment or taking classes (measured by Goal Attainment Scaling methodology). Secondary outcomes are reduced avoidance/increased activation (measured by the Behavioral Activation for Depression Scale), and increased environmental interactions (measured by the EROS: Environmental Rewards Observation Scale). Finally, they will develop training and supervision manuals to guide implementation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hiv, Fatigue, Goals
Keywords
HIV+, fatigue, return to work

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
46 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Behavioral activation therapy
Arm Type
Experimental
Arm Description
The Behavioral Activation Program for Energy and Productivity (BA-PEP) is a manualized, 8-session intervention, scheduled to coincide with maintenance armodafinil treatment. It is a structured counseling program with homework, short-term activities and goals, and includes problem-solving, identification of barriers and strategies for their resolution, with an ongoing focus on achieving employment or training.
Arm Title
supportive counseling (SC)
Arm Type
Placebo Comparator
Arm Description
Supportive counseling is designed to create an empathic, accepting environment, to direct attention to the patient's feelings and to facilitate acceptance of affective experience using supportive statements, reflective listening and empathic communications.
Intervention Type
Behavioral
Intervention Name(s)
Behavioral Activation Therapy
Other Intervention Name(s)
BA
Intervention Description
8 session, manualized intervention. Homework, short-term activities and goals specified, problem solving skills.
Intervention Type
Behavioral
Intervention Name(s)
Supportive Counseling
Intervention Description
8 sessions of manualized supportive counseling. Frequency and duration are designed to match the Behavioral Activation arm.
Primary Outcome Measure Information:
Title
Employment or enrollment in vocational classes as measured by Goal Attainment Scaling
Description
Goal Attainment Scaling assesses degree of success in reaching a pre-specified set of goals initially enumerated at study entry, with a 5-point score range. A score of zero is assigned to success in attaining the specified goal, with 2 greater and 2 lesser levels of accomplishment also specified.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Increased environmental interactions as measured by the EROS: Environmental Rewards Observation Scale.
Description
This is a standardized 10-item scale with a 4-point agree/disagree response format.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV+, ages 18-70 Under the care of a medical provider Clinically significant fatigue Speaks English Able and willing to give informed consent Patient seeks either work or vocational training but is blocked from doing so by current fatigue Exclusion Criteria: Primary care provider does not approve of study participation Medical rule-outs such as anemia, hypothyroidism, hypogonadism or other condition that may account for fatigue Abnormal EKG Untreated major depressive disorder; psychosis, bipolar disorder Current substance abuse/dependence Clinically significant suicidal ideation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Judith G Rabkin, PhD
Organizational Affiliation
New York State Psychiatric Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
New York State Psychiatric Institute
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
20492840
Citation
Rabkin JG, McElhiney MC, Rabkin R, McGrath PJ. Modafinil treatment for fatigue in HIV/AIDS: a randomized placebo-controlled study. J Clin Psychiatry. 2010 Jun;71(6):707-15. doi: 10.4088/JCP.09m05171bro. Epub 2010 May 4.
Results Reference
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Behavioral Activation/Armodafinil to Treat Fatigue in HIV/AIDS

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