Psychosocial Intervention for Older HIV+ Adults With HAND (IN-HAND)
Primary Purpose
HIV/AIDS, Aging, Mild Cognitive Impairment
Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
CRGT
HIV group therapy
Sponsored by
About this trial
This is an interventional supportive care trial for HIV/AIDS focused on measuring HIV-Associated Neurocognitive Disorder (HAND), Cognitive remediation group therapy, Mutual aid group therapy
Eligibility Criteria
Inclusion Criteria:
- Male or female; aged ≥ 40 years
- Documented HAND diagnosis of Mild Neurocognitive Disorder (MND)
- ≥ 5 years of HIV infection
- Provided consent to St. Michael's Hospital to be contacted for future research studies
- Can feasibly attend 8 weeks of group therapy in downtown Toronto
Exclusion Criteria:
- Documented HAND diagnosis of asymptomatic neurocognitive impairment (ANI) or HIV-associated dementia (HAD)
- Hospitalization within past 1 month
- Inability to communicate in English
- Inability to use a tablet
- Anyone deemed by the principal investigator to be disruptive to a support group setting
Sites / Locations
- AIDS Committee of Toronto (ACT)
- St. Michael's Hospital Neurobehavioral Research UnitRecruiting
- University Health Network, Toronto General Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Cognitive remediation group therapy
Mutual aid support group
Arm Description
8 weekly 3-hour sessions of CRGT
8 weekly 3-hour sessions of HIV group therapy
Outcomes
Primary Outcome Measures
Feasibility - participant attendance at group sessions
The sampling frame is approximately 100 people. The following targets (all based on a denominator of 100) would need to be met for a larger study to be considered feasible: ▁(>)30% of those contacted agree to participate, ▁(>)25% complete the pre-test, ▁(>)20% attend the first session, ▁(>)16% complete the full series and complete the post-test. Each participant must attend 80% (8/10) of the group sessions to be considered as completing the series.
Acceptability - participant satisfaction with group sessions
Participants will complete the Helping Characteristics of Self-Help and Support Groups Measure that will be complemented by questions about session length, number of sessions, activities used, and evaluation of facilitators.
Secondary Outcome Measures
Intervention fidelity - how closely facilitators adhere to intervention model
Facilitators of both study arms will submit weekly session reports. These reports will include checklists of the therapy components; use of an average 80% of components listed will be considered as good fidelity. These reports will also include open-ended questions about the sessions, including questions on group dynamics, challenges faced, and detail on activities used.
Full Information
NCT ID
NCT03483740
First Posted
January 9, 2018
Last Updated
April 9, 2018
Sponsor
University Health Network, Toronto
Collaborators
CIHR Canadian HIV Trials Network, Unity Health Toronto, AIDS Committee of Toronto, Factor-Inwentash Faculty of Social Work, University of Toronto
1. Study Identification
Unique Protocol Identification Number
NCT03483740
Brief Title
Psychosocial Intervention for Older HIV+ Adults With HAND
Acronym
IN-HAND
Official Title
Cognitive Remediation Group Therapy to Improve Older Adults' Ability to Cope With HIV-Associated Neurocognitive Disorder (HAND)
Study Type
Interventional
2. Study Status
Record Verification Date
April 2018
Overall Recruitment Status
Unknown status
Study Start Date
April 9, 2018 (Actual)
Primary Completion Date
October 31, 2018 (Anticipated)
Study Completion Date
December 31, 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
Collaborators
CIHR Canadian HIV Trials Network, Unity Health Toronto, AIDS Committee of Toronto, Factor-Inwentash Faculty of Social Work, University of Toronto
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
CTNPT 029 will test the feasibility and acceptability of cognitive remediation group therapy in older adults living with HIV who have been diagnosed with HIV-associated neurocognitive disorder (HAND). The cognitive remediation therapy will include tablet-based cognitive training and mindfulness-based stress reduction sessions.
Detailed Description
Approximately half of the aging HIV-positive population will be affected by HAND, making cognitive impairment related to HIV a significant comorbidity in this population. With the development, access to, and early initiation of modern antiretroviral therapy (ART), HAND is less severe and less common than it once was. However, people who were treated with old therapies, ones that were less effective and with higher rates of toxicity compared to current regimens, or who experienced AIDS defining illnesses, may be affected by HAND more frequently and more severely. Issues with cognition, memory, processing new information, problem solving, and decision making are all potential symptoms.
Psychosocial interventions have been used to decrease stress and depression and improve coping and quality of life in the general aging population experiencing cognitive impairment and depression. These techniques, which can vary widely, have not been fully tested in people aging with HAND.
CTNPT 029 (a pilot trial funded by the CTN) seeks to enroll 16 people at St. Michael's Hospital in Toronto. Study participants will be randomized to either receive cognitive remediation group therapy (CRGT) or standard HIV group therapy (control group). Both group therapies consist of a series of weekly 3-hour sessions led by a certified social worker and a peer. The CRGT group will spend one hour per session on brain training exercises (PositScience Software) and the remaining two hours on mindfulness-based stress reduction (meditation, breathing exercises, etc.). The control group will focus on general health and wellbeing for people aging with HIV. Study investigators will determine the usefulness of the structure of the sessions and the feasibility and acceptability of performing a study of this kind.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV/AIDS, Aging, Mild Cognitive Impairment, Group, Peer
Keywords
HIV-Associated Neurocognitive Disorder (HAND), Cognitive remediation group therapy, Mutual aid group therapy
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a pilot, parallel design, randomized, controlled trial (RCT) that will allocate a sample (n=16) of people (≥ 40 yrs old) aging with HIV who have been diagnosed with MND from St. Michael's Hospital (SMH) in Toronto to either arm 1: 8 weekly 3-hour sessions of CRGT; or arm 2: 8 weekly 3-hour sessions of HIV group therapy.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
16 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Cognitive remediation group therapy
Arm Type
Experimental
Arm Description
8 weekly 3-hour sessions of CRGT
Arm Title
Mutual aid support group
Arm Type
Active Comparator
Arm Description
8 weekly 3-hour sessions of HIV group therapy
Intervention Type
Behavioral
Intervention Name(s)
CRGT
Intervention Description
Cognitive remediation group therapy (CRGT) will be comprised of 1/3 brain training exercises on tablets using PositScience software by BrainHQ and 2/3 mindfulness-based stress reduction (MBSR) involving various activities such as meditation, breathing exercises, etc. Intervention will comprise of 8 weekly 3-hour sessions.
Intervention Type
Behavioral
Intervention Name(s)
HIV group therapy
Intervention Description
These groups use a model of mutual aid to encourage peer-based discussion on the effects of living with HIV. Topics are determined by the group; facilitators ensure that safety is maintained throughout and make connections between participants as appropriate. Intervension will comprise of 8 weekly 3-hour sessions.
Primary Outcome Measure Information:
Title
Feasibility - participant attendance at group sessions
Description
The sampling frame is approximately 100 people. The following targets (all based on a denominator of 100) would need to be met for a larger study to be considered feasible: ▁(>)30% of those contacted agree to participate, ▁(>)25% complete the pre-test, ▁(>)20% attend the first session, ▁(>)16% complete the full series and complete the post-test. Each participant must attend 80% (8/10) of the group sessions to be considered as completing the series.
Time Frame
Three months
Title
Acceptability - participant satisfaction with group sessions
Description
Participants will complete the Helping Characteristics of Self-Help and Support Groups Measure that will be complemented by questions about session length, number of sessions, activities used, and evaluation of facilitators.
Time Frame
Three months
Secondary Outcome Measure Information:
Title
Intervention fidelity - how closely facilitators adhere to intervention model
Description
Facilitators of both study arms will submit weekly session reports. These reports will include checklists of the therapy components; use of an average 80% of components listed will be considered as good fidelity. These reports will also include open-ended questions about the sessions, including questions on group dynamics, challenges faced, and detail on activities used.
Time Frame
Three months
Other Pre-specified Outcome Measures:
Title
Change in stress
Description
Assessed by the 'HIV/AIDS Stress Scale' at three time points. Score from 0 to 116. Lower scores mean better outcomes.
Time Frame
Baseline visit (week -1), follow-up visit (week 9), and end of study visit (week 21)
Title
Sustained use of brain training activities
Description
Self-report at three time points
Time Frame
Baseline visit (week -1), follow-up visit (week 9), and end of study visit (week 21)
Title
Sustained use of mindfulness strategies
Description
Assessed by the 'Five Facet Mindfulness Questionnaire - Short Form' at three time points. Score from 24 to 120. Higher scores mean better outcomes.
Time Frame
Baseline visit (week -1), follow-up visit (week 9), and end of study visit (week 21). Score from 0 to 26
Title
Change in anxiety
Description
Assessed by the 'Anxiety in Cognitive Impairment and Dementia Scale' at three time points. Score from 0 to 26. Lower scores mean better outcomes.
Time Frame
Baseline visit (week -1), follow-up visit (week 9), and end of study visit (week 21)
Title
Change in coping
Description
Assessed by the 'Coping Self-Efficacy Scale of Health Problems' at three time points. Score from 0 to 30. Higher scores mean better outcomes.
Time Frame
Baseline visit (week -1), follow-up visit (week 9), and end of study visit (week 21)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Male or female; aged ≥ 40 years
Documented HAND diagnosis of Mild Neurocognitive Disorder (MND)
≥ 5 years of HIV infection
Provided consent to St. Michael's Hospital to be contacted for future research studies
Can feasibly attend 8 weeks of group therapy in downtown Toronto
Exclusion Criteria:
Documented HAND diagnosis of asymptomatic neurocognitive impairment (ANI) or HIV-associated dementia (HAD)
Hospitalization within past 1 month
Inability to communicate in English
Inability to use a tablet
Anyone deemed by the principal investigator to be disruptive to a support group setting
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Andrew D Eaton, MSW
Phone
4163408484
Ext
283
Email
aeaton@actoronto.org
First Name & Middle Initial & Last Name or Official Title & Degree
Sharon L Walmsley, MD
Phone
4163403871
Email
sharon.walmsley@uhn.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sharon L Walmsley, MD
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
AIDS Committee of Toronto (ACT)
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4Y1Y5
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Galo F Ginocchio
Email
gginocchio@actoronto.ca
First Name & Middle Initial & Last Name & Degree
Andrew D Eaton, MSW
Facility Name
St. Michael's Hospital Neurobehavioral Research Unit
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B1M4
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Teri Sota, PhD
Phone
4168646060
Ext
6484
Email
sotat@smh.ca
First Name & Middle Initial & Last Name & Degree
Sean B Rourke, PhD
Facility Name
University Health Network, Toronto General Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2N2
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chantale Sheehan
Email
Chantale.Sheehan@uhn.ca
First Name & Middle Initial & Last Name & Degree
Sharon Walmsley, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
31676660
Citation
Eaton AD, Walmsley SL, Craig SL, Rourke SB, Sota T, McCullagh JW, Fallon BA. Protocol for a pilot randomised controlled trial evaluating feasibility and acceptability of cognitive remediation group therapy compared with mutual aid group therapy for people ageing with HIV-associated neurocognitive disorder (HAND) in Toronto, Canada. BMJ Open. 2019 Oct 31;9(10):e033183. doi: 10.1136/bmjopen-2019-033183.
Results Reference
derived
Links:
URL
http://www.hivnet.ubc.ca/clinical-trials/ctnpt-029/
Description
Plain language summary
Learn more about this trial
Psychosocial Intervention for Older HIV+ Adults With HAND
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