Offering Support and Electronic Resources for Care Partners of Those With Multiple Sclerosis
Primary Purpose
Multiple Sclerosis, Caregivers
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Tele-coaching
Website
Sponsored by

About this trial
This is an interventional supportive care trial for Multiple Sclerosis
Eligibility Criteria
Inclusion Criteria:
- An adult family member or friend (18 years of age or older) of a person with MS
- Self-identified as an unpaid caregiver for person with MS
- Access to internet
- Capable of providing informed consent in English
Exclusion Criteria:
- Under age 18
- Cannot speak English
- Unable to provide consent
- No access to the internet
Sites / Locations
- Case Western Reserve University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
High resource tailored intervention
Low-resource web-only intervention
Arm Description
Tele-coaching arm
Website arm
Outcomes
Primary Outcome Measures
anxiety, depression, and stress (DASS-42)
Change from baseline in anxiety, depression, and stress levels. Each of the three DASS scales contains 14 items. Using a 4-point Likert scale, scores range from 0- 42 for each scale. Higher scores indicate more depression, anxiety, and stress.
Secondary Outcome Measures
COVID specific anxiety (CAS scale)
Change from baseline in COVID specific anxiety. Using a 5-point scale, from 0 (not at all) to 4 (nearly every day), total score ranges from 0-20 while individual items range from 0-4. Higher scores indicate higher anxiety.
Full Information
NCT ID
NCT04662008
First Posted
December 2, 2020
Last Updated
March 18, 2022
Sponsor
Case Western Reserve University
1. Study Identification
Unique Protocol Identification Number
NCT04662008
Brief Title
Offering Support and Electronic Resources for Care Partners of Those With Multiple Sclerosis
Official Title
CLOSER_MS: Communicating With Local or Distance Caregivers Offering Support and Electronic Resources
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
March 10, 2021 (Actual)
Primary Completion Date
March 7, 2022 (Actual)
Study Completion Date
March 7, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Case Western Reserve University
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
This study is an enhancement of the Fatigue Management Programs for People with MS study (NCT03550170). The purpose of this randomized clinical trial is to test the effectiveness of two interventions delivered remotely to support unpaid caregivers (UC) of people with multiple sclerosis (MS). We hypothesize that a high resource intervention will be significantly better than a lower resource intervention in terms of the primary outcome (UC anxiety, depression, and stress) and secondary outcome (COVID specific anxiety).
Detailed Description
UCs are often caring for persons with chronic disabling conditions, who are at higher risk for severe COVID-19 illness. This presents incredibly stressful situations for UCs, which can result in depression, anxiety, and worse health outcomes both for them and their care recipients. Until a vaccine becomes available, these demands will force UCs to provide more support, whether in-person or remotely, for persons with MS. The aim of this study is to compare 2 modes of supporting UCs of people with MS. We will compare the effectiveness of a high resource highly tailored intervention that includes tele-coaching intervention (delivered via videoconference or phone) + web site information to a low-resource web-site only intervention. Our primary outcomes are UC anxiety, depression, and stress (DASS-42 scale) and a secondary outcome is COVID specific anxiety (CAS scale). These 2 interventions were selected because they will inform administrators and clinicians on whether a resource-intensive or a low-resource intervention is needed to yield meaningful outcomes. The comparison will also help UC decide how they should spend their limited time. These interventions are relevant to UCs of people with MS because of their need for tailored information provided in flexible ways to promote learning and support.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis, Caregivers
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
151 (Actual)
8. Arms, Groups, and Interventions
Arm Title
High resource tailored intervention
Arm Type
Active Comparator
Arm Description
Tele-coaching arm
Arm Title
Low-resource web-only intervention
Arm Type
Active Comparator
Arm Description
Website arm
Intervention Type
Behavioral
Intervention Name(s)
Tele-coaching
Intervention Description
This intervention arm will receive 4 one-to-one tele-coaching sessions facilitated by an advanced practice social worker. The sessions will take place over a 6-week period and will begin with a needs assessments to allow for tailoring of the intervention sessions. The sessions will include information and support in the areas of: general MS information, strategies for caring for a loved one with MS, MS and Covid (care strategies), caring for yourself, and planning for the future. The intervention will take place using Zoom videoconferencing technology or via telephone- per subject preference. In addition, all subjects will receive access to a study-specific website. The website will have links to publicly available information including general information about MS, online information, self-care, communication, caregiving, COVID-19, future planning.
Intervention Type
Behavioral
Intervention Name(s)
Website
Intervention Description
This intervention arm will receive access to a study-specific website. The website will have links to publicly available information including: general information about MS, online information, self-care, communication, caregiving, COVID-19, future planning.
Primary Outcome Measure Information:
Title
anxiety, depression, and stress (DASS-42)
Description
Change from baseline in anxiety, depression, and stress levels. Each of the three DASS scales contains 14 items. Using a 4-point Likert scale, scores range from 0- 42 for each scale. Higher scores indicate more depression, anxiety, and stress.
Time Frame
Each subject will be given the assessments at 3 points during the study: baseline, 6 weeks, and 12 weeks
Secondary Outcome Measure Information:
Title
COVID specific anxiety (CAS scale)
Description
Change from baseline in COVID specific anxiety. Using a 5-point scale, from 0 (not at all) to 4 (nearly every day), total score ranges from 0-20 while individual items range from 0-4. Higher scores indicate higher anxiety.
Time Frame
Each subject will be given the assessments at 3 points during the study: baseline, 6 weeks, and 12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
An adult family member or friend (18 years of age or older) of a person with MS
Self-identified as an unpaid caregiver for person with MS
Access to internet
Capable of providing informed consent in English
Exclusion Criteria:
Under age 18
Cannot speak English
Unable to provide consent
No access to the internet
Facility Information:
Facility Name
Case Western Reserve University
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44124
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34435971
Citation
Douglas SL, Plow M, Packer T, Lipson AR, Lehman MJ. Psychoeducational Interventions for Caregivers of Persons With Multiple Sclerosis: Protocol for a Randomized Trial. JMIR Res Protoc. 2021 Aug 26;10(8):e30617. doi: 10.2196/30617.
Results Reference
derived
Learn more about this trial
Offering Support and Electronic Resources for Care Partners of Those With Multiple Sclerosis
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