- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06001541
Web-based Program to Improve Self-management Among Veterans-caregiver Dyads (Web-SUCCEED)
A Web-based Program to Improve Chronic Illness Self-management by Engaging Patients and Informal Caregivers
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: For the 80% of older Americans who have at least one chronic condition, sharing self-management responsibilities with caregivers (relatives or friends) predicts longevity, better health, better quality of life, and fewer hospitalizations. Caregivers often support patients in their self-management efforts. This can bring patients and caregivers closer but can also generate stress for both that can interfere with self-management. Yet, self-management programs rarely support the coping needs of patient-caregiver dyads.
Significance: There are more than 5 million caregivers of Veterans; 75% of older Veterans receive some caregiver support. Caregivers incur individual financial and emotional costs even as they provide unpaid care. Having an effective self-management strategy that addresses the needs of both can improve outcomes and quality of life for millions of Veterans who suffer from chronic illnesses and their caregivers. This project addresses the priorities "Long-term care and Caregiving," "Virtual Care/Telehealth," and "Access to Care" and is consistent with the legislative goals of the MISSION Act.
Innovation and Impact: This highly innovative proposal uses the novel concept that strengthening the interpersonal relationships between Veterans and caregivers can improve the self-management of chronic conditions. It challenges current clinical paradigms by addressing the collective stress coping needs of dyads. It is methodologically innovative because unlike many behavioral intervention trials, it assesses barriers and facilitators to plan for future implementation. The focus on technology-enabled tools is timely given how COVID19 has transformed care delivery. This project takes advantage of the unique capabilities of the VA health system to explore questions including robust caregiver support and virtual care programs.
Specific Aims: With investments from VA HSR&D, the investigators have developed and successfully pilot tested a new theoretically-derived technology called Web-based Self-care Using Collaborative Coping EnhancEment in Diseases (web-SUCCEED). We propose to conduct a randomized clinical trial comparing web-SUCCEED to an enhanced usual care (EUC) control. The investigators will conduct a formative evaluation guided by the Consolidated Framework of Implementation Research (CFIR) to accelerate future implementation.
1. Assess whether web-SUCCEED improves Veteran outcomes of self-management compared to EUC, 4 weeks and 6 months following randomization.
2a. Assess whether web-SUCCEED improves patient stress and quality of life. 2b. Assess whether web-SUCCEED improves caregiver stress, quality of life and caregiver burden.
2c. Examine communication, dyadic coping, mutuality, and relationship quality as mediators of primary and secondary outcomes (Aims 1, 2a, 2b).
3. Guided by CFIR, conduct a formative evaluation involving key stakeholder interviews to understand barriers and facilitators of future implementation.
Methodology: The investigators will recruit 280 cognitively intact Veterans from VA Palo Alto Health Care System who are managing at least one common chronic condition, and their caregivers. Veteran-caregiver dyads will be randomized 1:1 to web-SUCCEED or EUC. Veteran and caregiver assessments will take place at baseline, then again at 4 weeks and 6 months. The formative evaluation will be guided by CFIR and involve semi-structured interviews with clinical staff, providers, and facility leaders in Year 4.
Next Steps: The formative evaluation will set the investigators up for implementation studies to evaluate web-SUCCEED in a wider array of clinical settings and facilities. Existing operational partnerships will facilitate wider clinical implementation and moving research into practice. The innovative project, strong investigative team and operational partnerships will ensure a successful study that has the potential to shift clinical paradigms.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Mary B Walsh, RN
- Phone Number: (412) 260-4289
- Email: mary.walsh3@va.gov
Study Locations
-
-
California
-
Palo Alto, California, United States, 94304-1207
- Recruiting
- VA Palo Alto Health Care System, Palo Alto, CA
-
Contact:
- Geoffrey W Goodale, BS
- Phone Number: 518-626-5626
- Email: Geoffrey.Goodale@va.gov
-
Principal Investigator:
- Ranak B Trivedi, PhD MA MS
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Participants will be medically eligible if they have been diagnosed with at least one common chronic condition considered responsive to outpatient management as defined by being on the AHRQ list of Patient Quality Indicators, which are conditions that are considered responsive to high quality outpatient care.
- The investigators will also include conditions that are disproportionately high among Veterans (pain, mental health conditions).
Based on the pilot study, the investigators anticipate this to include:
- musculoskeletal pain
- cardiovascular disease
- diabetes
- kidney disease
- depression
Eligible participants will have at least one outpatient visit in the prior 12 months related to their diagnosis and have a primary caregiver who lives with the Veteran. Dyads will be excluded if either the Veterans or their caregiver:
- 1) have an implantable cardioverter defibrillator
- 2) are on hemodialysis
- 3) have received an organ transplant or are waitlisted for one
- 4) are undergoing chemotherapy or radiation for cancer
- 5) have limited life expectancy as determined by the provider or hospice care
- 6) have dementia or other major cognitive deficits
- 7) have a substance use disorder (SUD), since supporting interpersonal relationships in SUDs require specialized training that is outside the scope of web-SUCCEED
- 8) have a paid caregiver who provides 50% or more support to the Veteran
- 9) are actively psychotic or suicidal. Due to content overlap, the investigators will exclude Veterans who have participated in the Stanford CDSMP program, and caregivers who have participated in the Building Better Caregiver program
Exclusion Criteria:
Dyads deemed eligible with these criteria will be further screened by the study staff for internet use, self-management distress, and interpersonal violence.
- a. Internet Use: The investigators will use the question that used in the pilot study, "How often do you use a computer?" The investigators will exclude dyads where either Veterans or caregivers answer "less than once a week."
b. Self-management Distress: The investigators will screen Veterans and caregivers for self-management distress using the same two-item measure that have been used for the pilot study of web-SUCCEED:
- 1) How overwhelmed do you feel by the demands of living with your [OR Veteran's] health condition(s)?
- 2) How often do you feel that you are failing in your routine to manage your [OR Veteran's] health conditions?" Respondents rate items from 1 (Not a problem) to 6 (A very serious problem), and scores are added. Dyads will be eligible if both individuals score a minimum of 2 and at least one scores >3.
- c. Interpersonal Violence: Veterans and caregivers will be separately screened with the question, "How do you and [Veteran, caregiver] handle stressful conversations or conflict?" If needed, this will be followed up with: "In the last year, has it gotten physical or have there been threats of physical force?". If the answer to the last question is "yes", dyads will not be eligible. Dr. Trivedi will assess for immediate safety, provide local resources, and involve authorities if appropriate. In the investigators' experience, this is a low likelihood event.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Web-SUCCEED+Enhanced Usual Care
web-SUCCEED, usual care, psychoeducational materials and resources for caregivers.
|
web-SUCCEED (Web-based Self-management Using Collaborative Coping EnhancEment in Diseases), a theoretically-derived, dyadic, self-management program.20,21
Web-SUCCEED is designed to improve self-management by improving dyadic stress coping and strengthening collaboration and communication.21
Web-SUCCEED comprises: 1) a three-module, self-paced behavioral intervention that Veterans and caregivers complete individually (one audio/video module per week) on the web-SUCCEED website; 2) brief, staff-led telephone calls in which dyads participate simultaneously after each module; and 3) peer support via a study-specific discussion board.
Dyads learn and practice cognitive behavioral skills to reduce individual and relationship stress; improve positive emotions; improve communication and collaboration; increase pleasant activities; and maintain behavior change.
|
|
Active Comparator: Enhanced Usual Care
Usual care, enhanced by psychoeducational materials and resources for caregivers.
|
web-SUCCEED (Web-based Self-management Using Collaborative Coping EnhancEment in Diseases), a theoretically-derived, dyadic, self-management program.20,21
Web-SUCCEED is designed to improve self-management by improving dyadic stress coping and strengthening collaboration and communication.21
Web-SUCCEED comprises: 1) a three-module, self-paced behavioral intervention that Veterans and caregivers complete individually (one audio/video module per week) on the web-SUCCEED website; 2) brief, staff-led telephone calls in which dyads participate simultaneously after each module; and 3) peer support via a study-specific discussion board.
Dyads learn and practice cognitive behavioral skills to reduce individual and relationship stress; improve positive emotions; improve communication and collaboration; increase pleasant activities; and maintain behavior change.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-care of Chronic Illness Inventory Change
Time Frame: Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
The SC-CII is based on the Middle Range Theory of Self-care.
[Across three 10-item scales, the SC-CII assesses self-care maintenance (i.e., health-promoting and illness-related behaviors such as treatment adherence), self-care monitoring (i.e., ability to track symptoms and signs of an illness such as shortness of breath), and self-care management (i.e., ability to take action to deal with symptoms such as taking a diuretic to relieve fluid build-up).
Coefficient alphas of the 3 subscales are: self-care monitoring (.81), self-care management (.71), and self-care maintenance (.67) in testing with patients with common chronic conditions.
Each scale is standardized to a score of 100, and scores of 70 or more on each scale indicate adequate self-management.
|
Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
PROMIS Profile-29 v2.0
Time Frame: Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
Common Data Element indexed in the PhenX Toolkit that measures quality of life.
|
Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
|
Caregiver Reaction Assessment
Time Frame: Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
Positive and negative caregiver experience.
|
Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
|
Perceived Stress Scale
Time Frame: Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
Self-reported stress measure from PROMIS, 10 items.
|
Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Couples Illness Communication Scale
Time Frame: Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
Self-reported measure of communication, 4 items.
|
Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
|
Pittsburgh Sleep Quality Index
Time Frame: Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
Measure of self-reported sleep quality.
|
Baseline (pre intervention), 6 week (post intervention), 6 month (follow-up)
|
Collaborators and Investigators
Investigators
- Principal Investigator: Ranak B Trivedi, PhD MA MS, VA Palo Alto Health Care System, Palo Alto, CA
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IIR 19-137
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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