Informal Caregivers ANSWERS-VA
Primary Purpose
Stroke, Traumatic Brain Injury
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ANSWERS - Acquiring New Skills While Enhancing Remaining Strengths
Control
Sponsored by
About this trial
This is an interventional health services research trial for Stroke focused on measuring stroke, Injury, Brain, Traumatic, Family Caregivers, TBI (Traumatic Brain Injury), Informal Caregivers
Eligibility Criteria
Inclusion Criteria:
- Informal caregiver of a family member or friend (Veteran) with a stroke or TBI
- Caregiver must express need or concerns in providing care
- Plans to be providing care for 1 year or longer
- Access to telephone
- Willingness to participate in 9 call from a nurse and 5 data collection calls at designated timepoints
- Veteran's stroke must be within past 3 years
- Veteran's TBI must be since 9/11/01
Exclusion Criteria:
- Caregiver or survivor age < 18 years
- Caregiver denies that survivor has had a stroke or a TBI
- Caregiver does not consider him or herself a caregiver, stating that the survivor is not impaired or is the same as before the stroke or TBI
- Caregiver has low task difficulty (OCBS task difficulty score < 16)
- Caregiver communication difficulties (e.g., hearing loss)
- Caregiver not fluent in the English language
- Caregiver with serious medical illness limiting ability to participate
- Caregiver refuses to sign a HIPAA authorization allowing the VA to store personal health information (PHI) in a location outside the VA
- Survivor residing in a nursing home or long-term care facility
- Survivor or caregiver has a terminal illness (e.g., cancer, end of life condition with decreased life expectancy, renal failure requiring dialysis)
- Survivor or caregiver history of hospitalization for alcohol or drug abuse
- Survivor or caregiver history of Alzheimer's, dementia, suicidal tendencies, severe untreated depression or manic depressive disorder, or schizophrenia.
- Survivor or caregiver pregnancy
- Survivor or caregiver is a prisoner or on house arrest
- Survivor had a Transient Ischemic Attack (rather than a hemorrhagic or ischemic stroke)
- Survivor had a stroke more than 3 years ago
Sites / Locations
- Richard L. Roudebush VA Medical Center, Indianapolis, IN
- Michael E. DeBakey VA Medical Center, Houston, TX
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
ANSWERS-VA
Control
Arm Description
8 week telephone intervention with nurse case manager using "Acquiring New Skills While Enhancing Remaining Strengths" (ANSWERS)
8 week telephone usual care with education with nurse case manager
Outcomes
Primary Outcome Measures
Caregiver's Depressive Symptoms by Patient Health Questionnaire (PHQ9) Scale
Depression scores are measured with the PHQ9 scale. Scores can range from 0 to 27, with higher scores indicating higher levels of depression.
Mediators of Caregiver's Task Difficulty
Task difficulty is measured with the Oberst Caregiving Burden Scale. Scores on a Likert scale can range from 1 to 5 with higher scores indicating higher levels of burden.
Mediators of Caregiver's Optimism Scale
Optimism is measured with the Life Orientation Test-Revised Scale. Scores can range from 0 to 40 with higher scores indicating more optimism.
Mediators of Caregiver's Threat Appraisal Scale
Threat appraisal is measured with the Appraisal of Caregiving Scale: Threat Subscale. Scores on a Likert scale can range from 1 to 5 with higher scores indicating less belief, feelings and ability to take care of a loved one with stroke or brain injury in the future.
Secondary Outcome Measures
Full Information
NCT ID
NCT02398409
First Posted
February 26, 2015
Last Updated
June 3, 2020
Sponsor
VA Office of Research and Development
1. Study Identification
Unique Protocol Identification Number
NCT02398409
Brief Title
Informal Caregivers ANSWERS-VA
Official Title
Telephone Assessment and Skill-Building Intervention for Informal Caregivers
Study Type
Interventional
2. Study Status
Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
November 3, 2014 (Actual)
Primary Completion Date
June 30, 2018 (Actual)
Study Completion Date
March 31, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine the effectiveness of the ANSWERS- VA intervention (Acquiring New Skills While Enhancing Remaining Strengths for Veterans) while also determining it's cost effectiveness in the stroke and traumatic brain injury (TBI) populations.
Detailed Description
Background: Stroke and traumatic brain injury (TBI) are leading causes of long-term disability among Veterans and result in the need for care from informal caregivers in the home setting. There are very few evidence-based, easy-to-deliver follow-up programs to train Veterans and caregivers across multiple domains post injury. The "Acquiring New Skills While Enhancing Remaining Strengths for Veterans (ANSWERS-VA)" intervention aims to provide the Veteran and caregiver dyad with a set of practical skills that each can use in coping with and managing symptoms of a brain injury, applying a strength-based approach.
Objectives: The objectives of this study are to conduct a randomized controlled trial (RCT) to evaluate (a) the efficacy of the ANSWERS-VA dyadic intervention with Veterans who have sustained a stroke and/or TBI and their informal caregivers, and (b) estimate effect sizes for the ANSWERS-VA intervention. The ANSWERS-VA intervention will be compared with an educational intervention that will serve as an attention control group.
Specific Aim 1: To tailor the implementation of the ANSWERS-VA intervention to dyads of Veterans post stroke and/or TBI and their informal caregivers (n=10) and modify the implementation processes for the RCT.
Specific Aim 2: To test the short-term (immediately post-intervention) and long-term, sustained (12 and 24 weeks, and at 1 year) efficacy of the ANSWERS-VA intervention for improving: (a) the primary outcomes of the caregivers' quality of life and unhealthy days, and (b) the caregiver mediators of task difficulty, threat appraisal, self-efficacy for caregiving, and optimism.
Specific Aim 3: To evaluate program delivery costs for the ANSWERS-VA intervention and the educational attention control procedures, and to assess the cost-effectiveness of the ANSWERS-VA intervention in terms of noncaregiving hours and unhealthy days in caregivers of Veterans post stroke and/or TBI.
Exploratory Aim 1: To estimate the effect sizes for the ANSWERS-VA intervention for the caregiver and Veteran on the secondary outcomes of depressive symptoms, social participation, and quality of the dyadic relationship.
Methods: The investigators propose to conduct a RCT to evaluate the ANSWERS-VA intervention among Veterans with stroke or TBI and their caregivers (dyads). Veterans with stroke (N = 222) or TBI (N = 108) and their informal caregivers, who have received care at the Michael E. DeBakey Veterans Affairs Medical Center in Houston or the Richard L. Roudebush VAMC in Indianapolis, will be randomized to the ANSWERS-VA intervention or to an attention control group. Both the intervention and control procedures involve 8 telephone sessions delivered over 8 weeks, with a booster session at 12 weeks. Data collections will occur at baseline, 8 weeks (short-term intervention effect), 12 weeks (after booster), 24 weeks, and 1 year after baseline (long-term sustainability of intervention effect). Linear mixed models will be applied to the repeated-measures data to test efficacy of the program in stroke caregivers and to estimate effect sizes in TBI caregivers. An incremental cost-effectiveness ratio will be employed to address the comparative costs and outcomes for the ANSWERS-VA intervention and attention control groups.
Status: Essential modifications for this project were requested and approved via VA Central Office. Institutional Review Board approval has been obtained for these modifications in Indianapolis and in Houston. Graduate students from multiple disciplines have been hired and have received two days of onsite training specific to the ANSWERS-VA intervention and control procedures, screening, recruitment, and data collection processes. The REDCap database has been updated for the project modifications and has been further tested. The investigators are currently working with frontline providers at both sites to recruit potential participants for this RCT. Enrollment of first subject dyads began November, 2014. At this time, the investigators have completed recruitment of new dyads. We continue to complete outcomes assessments on some dyads. We plan to submit an abstract to the International Stroke Conference in January 2019.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Traumatic Brain Injury
Keywords
stroke, Injury, Brain, Traumatic, Family Caregivers, TBI (Traumatic Brain Injury), Informal Caregivers
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
143 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ANSWERS-VA
Arm Type
Experimental
Arm Description
8 week telephone intervention with nurse case manager using "Acquiring New Skills While Enhancing Remaining Strengths" (ANSWERS)
Arm Title
Control
Arm Type
Other
Arm Description
8 week telephone usual care with education with nurse case manager
Intervention Type
Behavioral
Intervention Name(s)
ANSWERS - Acquiring New Skills While Enhancing Remaining Strengths
Intervention Description
Randomized trial to evaluate the efficacy of the telephone intervention "Acquiring New Skills While Enhancing Remaining Strengths"in informal caregivers of Veterans with stroke and TBI.
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
8 week telephone usual care with education with nurse case manager
Primary Outcome Measure Information:
Title
Caregiver's Depressive Symptoms by Patient Health Questionnaire (PHQ9) Scale
Description
Depression scores are measured with the PHQ9 scale. Scores can range from 0 to 27, with higher scores indicating higher levels of depression.
Time Frame
Baseline, Week 12, 6 months and 1 year
Title
Mediators of Caregiver's Task Difficulty
Description
Task difficulty is measured with the Oberst Caregiving Burden Scale. Scores on a Likert scale can range from 1 to 5 with higher scores indicating higher levels of burden.
Time Frame
Baseline, Week 12, 6 months and 1 year
Title
Mediators of Caregiver's Optimism Scale
Description
Optimism is measured with the Life Orientation Test-Revised Scale. Scores can range from 0 to 40 with higher scores indicating more optimism.
Time Frame
Baseline, Week 12, 6 months and 1 year
Title
Mediators of Caregiver's Threat Appraisal Scale
Description
Threat appraisal is measured with the Appraisal of Caregiving Scale: Threat Subscale. Scores on a Likert scale can range from 1 to 5 with higher scores indicating less belief, feelings and ability to take care of a loved one with stroke or brain injury in the future.
Time Frame
Baseline, Week 12, 6 months and 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Informal caregiver of a family member or friend (Veteran) with a stroke or TBI
Caregiver must express need or concerns in providing care
Plans to be providing care for 1 year or longer
Access to telephone
Willingness to participate in 9 call from a nurse and 5 data collection calls at designated timepoints
Veteran's stroke must be within past 3 years
Veteran's TBI must be since 9/11/01
Exclusion Criteria:
Caregiver or survivor age < 18 years
Caregiver denies that survivor has had a stroke or a TBI
Caregiver does not consider him or herself a caregiver, stating that the survivor is not impaired or is the same as before the stroke or TBI
Caregiver has low task difficulty (OCBS task difficulty score < 16)
Caregiver communication difficulties (e.g., hearing loss)
Caregiver not fluent in the English language
Caregiver with serious medical illness limiting ability to participate
Caregiver refuses to sign a HIPAA authorization allowing the VA to store personal health information (PHI) in a location outside the VA
Survivor residing in a nursing home or long-term care facility
Survivor or caregiver has a terminal illness (e.g., cancer, end of life condition with decreased life expectancy, renal failure requiring dialysis)
Survivor or caregiver history of hospitalization for alcohol or drug abuse
Survivor or caregiver history of Alzheimer's, dementia, suicidal tendencies, severe untreated depression or manic depressive disorder, or schizophrenia.
Survivor or caregiver pregnancy
Survivor or caregiver is a prisoner or on house arrest
Survivor had a Transient Ischemic Attack (rather than a hemorrhagic or ischemic stroke)
Survivor had a stroke more than 3 years ago
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Virginia (Ginger) S. Wilder, PhD MSN RN
Organizational Affiliation
Richard L. Roudebush VA Medical Center, Indianapolis, IN
Official's Role
Principal Investigator
Facility Information:
Facility Name
Richard L. Roudebush VA Medical Center, Indianapolis, IN
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202-2884
Country
United States
Facility Name
Michael E. DeBakey VA Medical Center, Houston, TX
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34813082
Citation
Crocker TF, Brown L, Lam N, Wray F, Knapp P, Forster A. Information provision for stroke survivors and their carers. Cochrane Database Syst Rev. 2021 Nov 23;11(11):CD001919. doi: 10.1002/14651858.CD001919.pub4.
Results Reference
derived
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