search
Back to results

Tele-Exercise and Multiple Sclerosis (TEAMS)

Primary Purpose

Multiple Sclerosis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
DirectCAM
TeleCAM
rDirectCAM
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Multiple Sclerosis focused on measuring Multiple Sclerosis, Yoga, Pilates, Telerehabilitation, Physical activity

Eligibility Criteria

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

Inclusion Criteria:

  • Physician permission to participate in the study
  • Mild to moderate disability (i.e., ambulate with/without assistive device, Patient-Determined Disease Steps [PDDS] 0 - 7
  • Able to use arms/legs for exercise

Exclusion Criteria:

  • Significant visual acuity that prevents seeing a tablet screen to follow home exercise program
  • Cardiovascular disease event within the last six months, several pulmonary disease, and/or renal failure
  • Active pressure ulcers
  • Currently pregnant
  • Within 30 days of receiving a rehabilitation program
  • Already meeting physical activity guidelines (GLTEQ > 24)

Sites / Locations

  • Upstream Rehabilitation Inc.
  • Upstream Rehabilitation Inc.
  • Tanner Foundation
  • Upstream Rehabilitation Inc.
  • Upstream Rehabilitation Inc.
  • Southeast Alabama Medical Center Rehabilitation Services
  • Gulf Coast Therapy
  • Gulf Coast Therapy
  • Encore Rehabilitation
  • Upstream Rehabilitation Inc.
  • Therapy Achievements
  • Upstream Rehabilitation Inc.
  • Upstream Rehabilitation Inc.
  • Gulf Coast Therapy
  • Montgomery East Physical Therapy
  • Upstream Rehabilitation Inc.
  • Encore Rehabilitation
  • Upstream Rehabilitation Inc.
  • Cornerstone Rehabilitation
  • Upstream Rehabilitation Inc.
  • Upstream Rehabilitation Inc.
  • Upstream Rehabilitation Inc.
  • Upstrem Rehabilitation
  • Upstream Rehabilitation Inc.
  • River City Rehabilitation
  • Encore Rehabilitation
  • Upstream Rehabilitation Inc.
  • Methodist Rehabilitation Center
  • Encore Rehabilitation
  • North Sunflower Medical Center
  • Cornerstone Rehabilitation
  • Upstream Rehabilitation Inc.
  • Upstream Rehabilitation Inc.
  • Cornerstone Rehabilitation
  • Upstream Rehabilitation Inc.
  • Upstream Rehabilitation Inc.
  • Upstream Rehabilitation Inc.
  • Upstream Rehabilitation Inc.
  • Upstream Rehabilitation Inc.
  • Upstream Rehabilitation Inc.

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

DirectCAM

TeleCAM

rDirectCAM

Arm Description

The DirectCAM arm receives the intervention content via therapists at participating clinics.

The TeleCAM arm receives the intervention content at home using pre-loaded tablets and Interactive Voice Response (IVR) system technology.

The rDirectCAM arm is being implemented in response to Covid-19. The rDirectCAM arm receives the intervention content delivered remotely in real-time by therapists via videoconferencing technology.

Outcomes

Primary Outcome Measures

Change in Baseline Pain at Month 3 and Month 12
Measured by 36-Item Short Form Survey (SF-36).
Change in Baseline Fatigue at Month 3 and Month 12
Measured by Modified Fatigue Impact Scale (MFIS).
Change in Baseline Quality of Life at Month 3 and Month 12
Measured by 36-Item Short Form Survey (SF-36).
Change in Baseline Physical Activity at Month 3 and Month 12
Measured by the Godin Leisure Time Exercise Questionnaire (GLTEQ).

Secondary Outcome Measures

Change in Baseline Balance at Month 3 and Month 12
Measured using the Berg Balance Scale (BBS).
Change in Baseline Endurance at Month 3 and Month 12
Measured using the 6-minute Walk Test (6MWT).
Change in Baseline Gait at Month 3 and Month 12
Measured using the Timed 25-Foot Walk (T25-FW).
Change in Baseline Strength at Month 3 and Month 12
Measured using a hand-held dynamometer.

Full Information

First Posted
April 5, 2017
Last Updated
April 25, 2023
Sponsor
University of Alabama at Birmingham
Collaborators
Patient-Centered Outcomes Research Institute, Alabama Neurology Associates, PC, Lakeshore Foundation
search

1. Study Identification

Unique Protocol Identification Number
NCT03117881
Brief Title
Tele-Exercise and Multiple Sclerosis
Acronym
TEAMS
Official Title
Comparative Effectiveness Trial Between a Clinic- and Home-Based Complementary and Alternative Medicine Telerehabilitation Intervention for Adults With Multiple Sclerosis (MS)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
January 8, 2018 (Actual)
Primary Completion Date
October 30, 2021 (Actual)
Study Completion Date
October 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alabama at Birmingham
Collaborators
Patient-Centered Outcomes Research Institute, Alabama Neurology Associates, PC, Lakeshore Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare the effects of two delivery models of an evidence-based complementary alternative medicine (CAM) program that combines neurorehabilitative (functional) exercise, yoga, and Pilates for adults age 18-70 with multiple sclerosis (MS). CAM will be delivered as a 12-week program through two different delivery forms: On-site at a clinic (DirectCAM) and telerehabilitation (TeleCAM). Participants will be randomly assigned to one of these two groups. **On March 16th, 2020, the University of Alabama at Birmingham halted all onsite non-essential research in response to the Covid-19 pandemic. Since then, the study has begun to conduct all testing remotely through videoconferencing technology. In addition, another study group, remote DirectCAM (rDirectCAM), has been incorporated into the study to continue the 12-week program delivery for newly recruited participants via videoconferencing technology.**
Detailed Description
There are few primary care and multiple sclerosis (MS) clinics that provide full exercise and rehabilitation services for patients with MS, especially in mostly rural, low-income areas such as Alabama, Mississippi, and Tennessee. Telerehabilitation, or the delivery of rehabilitation services over the telephone and/or the Internet, can help fill service gaps for underserved MS patient populations in this region. The proposed study will determine if our evidence-based rehabilitation and exercise program produces similar health outcomes when delivered in clinic or at home, using pre-loaded tablets and Interactive Voice Response (IVR) system technology among 759 participants with MS from 40 clinics across Alabama, Mississippi, and Tennessee. **In response to the Covid-19 pandemic, the study aims to recruit 74 participants with MS into the rDirectCAM, where the 12-week program is delivered in real-time via videoconferencing technology. The rDirectCAM will determine if a telehealth rehabilitation program can have a similar effect as when the program is offered in person.** The outcomes that we hope to achieve through the proposed rehabilitation and exercise program, referred to as complementary alternative medicine, are improved physical activity, decreased pain and fatigue, and quality of life. We also seek to improve attitudes and behaviors related to physical activity, such as outcome expectations for physical activity, social support from family and friends for physical activity, self-efficacy (i.e., confidence in one's ability to be active), and self-regulation (i.e., setting exercise goals). We will examine the variation in outcomes by patient characteristics such as age and severity of disability to determine for whom the intervention is effective. This project is important to patients with MS because it seeks to reduce their barriers to receiving exercise treatment and increase the convenience and appeal of such programs through technology. Furthermore, findings and resources from this study will be quickly provided to MS patients and clinicians across the United States (e.g., via training webinars through our National Center on Health, Physical Activity, and Disability [NCHPAD]) and thereby improve the quality and reach of exercise treatment for patients with MS. The patient and stakeholder partners include MS patients, caretakers, and clinicians, who have been actively guiding the development of this project. In stakeholder meetings, members have provided insight into exercise treatment needs and preferences (e.g., individually tailored approaches that account for varying levels of mobility); outcomes of interest to the patient population (e.g., pain, fatigue, quality of life); and strategies for engaging/motivating participants with MS who may be discouraged and experiencing fatigue and pain (e.g., IVR calls and feedback). Moreover, their ongoing program satisfaction feedback will be important to our recruitment and retention success. Finally, the stakeholders will help make this project successful by continuing to emphasize the importance of long-term gains in health outcomes and promote (through NCHPAD) the sustainability of the program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Multiple Sclerosis, Yoga, Pilates, Telerehabilitation, Physical activity

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
912 (Actual)

8. Arms, Groups, and Interventions

Arm Title
DirectCAM
Arm Type
Experimental
Arm Description
The DirectCAM arm receives the intervention content via therapists at participating clinics.
Arm Title
TeleCAM
Arm Type
Experimental
Arm Description
The TeleCAM arm receives the intervention content at home using pre-loaded tablets and Interactive Voice Response (IVR) system technology.
Arm Title
rDirectCAM
Arm Type
Experimental
Arm Description
The rDirectCAM arm is being implemented in response to Covid-19. The rDirectCAM arm receives the intervention content delivered remotely in real-time by therapists via videoconferencing technology.
Intervention Type
Behavioral
Intervention Name(s)
DirectCAM
Intervention Description
The intervention consists of a 60-minute Complementary Alternative Medicine (CAM) program that includes yoga, Pilates and dual-functioning exercises, which is delivered 2 times per week for the first 8 weeks and 1 time per week for the following 4 weeks at a clinic with a therapist. At the end of week 12, participants will be asked to continue the program in their home for up to 1 year post-intervention using handouts.
Intervention Type
Behavioral
Intervention Name(s)
TeleCAM
Intervention Description
The intervention consists of a 60-minute Complementary Alternative Medicine (CAM) program that includes yoga, Pilates and dual-functioning exercises, which is delivered 2 times per week for the first 8 weeks and 1 time per week for the following 4 weeks at home via videos. At the end of week 12, participants will be asked to continue the program in their home for up to 1 year post-intervention using the videos.
Intervention Type
Behavioral
Intervention Name(s)
rDirectCAM
Intervention Description
The intervention consists of a 60-minute Complementary Alternative Medicine (CAM) program that includes yoga, Pilates and dual-functioning exercises, which is delivered 2 times per week for the first 8 weeks and 1 time per week for the following 4 weeks by a therapist via videoconferencing technology. At the end of week 12, participants will be asked to continue the program in their home for up to 1 year post-intervention using handouts.
Primary Outcome Measure Information:
Title
Change in Baseline Pain at Month 3 and Month 12
Description
Measured by 36-Item Short Form Survey (SF-36).
Time Frame
48 weeks
Title
Change in Baseline Fatigue at Month 3 and Month 12
Description
Measured by Modified Fatigue Impact Scale (MFIS).
Time Frame
48 weeks
Title
Change in Baseline Quality of Life at Month 3 and Month 12
Description
Measured by 36-Item Short Form Survey (SF-36).
Time Frame
48 weeks
Title
Change in Baseline Physical Activity at Month 3 and Month 12
Description
Measured by the Godin Leisure Time Exercise Questionnaire (GLTEQ).
Time Frame
48 weeks
Secondary Outcome Measure Information:
Title
Change in Baseline Balance at Month 3 and Month 12
Description
Measured using the Berg Balance Scale (BBS).
Time Frame
48 weeks
Title
Change in Baseline Endurance at Month 3 and Month 12
Description
Measured using the 6-minute Walk Test (6MWT).
Time Frame
48 weeks
Title
Change in Baseline Gait at Month 3 and Month 12
Description
Measured using the Timed 25-Foot Walk (T25-FW).
Time Frame
48 weeks
Title
Change in Baseline Strength at Month 3 and Month 12
Description
Measured using a hand-held dynamometer.
Time Frame
48 weeks
Other Pre-specified Outcome Measures:
Title
Outcome expectations for exercise
Description
Measured by the Multidimensional Outcome Expectations for Exercise Scale (MOEES).
Time Frame
48 weeks
Title
Exercise self-efficacy
Description
Measured by the Exercise Self-efficacy Scale.
Time Frame
48 weeks
Title
Social support for exercise
Description
Measured by the Social Provisions Scale.
Time Frame
48 weeks
Title
Exercise self-regulation
Description
Measured by the Exercise Goal-setting Scale.
Time Frame
48 weeks

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: Physician permission to participate in the study Mild to moderate disability (i.e., ambulate with/without assistive device, Patient-Determined Disease Steps [PDDS] 0 - 7 Able to use arms/legs for exercise Exclusion Criteria: Significant visual acuity that prevents seeing a tablet screen to follow home exercise program Cardiovascular disease event within the last six months, several pulmonary disease, and/or renal failure Active pressure ulcers Currently pregnant Within 30 days of receiving a rehabilitation program Already meeting physical activity guidelines (GLTEQ > 24)
Facility Information:
Facility Name
Upstream Rehabilitation Inc.
City
Athens
State/Province
Alabama
ZIP/Postal Code
35613
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Bessemer
State/Province
Alabama
ZIP/Postal Code
35022
Country
United States
Facility Name
Tanner Foundation
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35209
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Calera
State/Province
Alabama
ZIP/Postal Code
35040
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Cullman
State/Province
Alabama
ZIP/Postal Code
35058
Country
United States
Facility Name
Southeast Alabama Medical Center Rehabilitation Services
City
Dothan
State/Province
Alabama
ZIP/Postal Code
36301
Country
United States
Facility Name
Gulf Coast Therapy
City
Fairhope
State/Province
Alabama
ZIP/Postal Code
36532
Country
United States
Facility Name
Gulf Coast Therapy
City
Foley
State/Province
Alabama
ZIP/Postal Code
36536
Country
United States
Facility Name
Encore Rehabilitation
City
Fort Payne
State/Province
Alabama
ZIP/Postal Code
35967
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Gadsden
State/Province
Alabama
ZIP/Postal Code
35906
Country
United States
Facility Name
Therapy Achievements
City
Huntsville
State/Province
Alabama
ZIP/Postal Code
35801
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Jacksonville
State/Province
Alabama
ZIP/Postal Code
36265
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Jasper
State/Province
Alabama
ZIP/Postal Code
35501
Country
United States
Facility Name
Gulf Coast Therapy
City
Mobile
State/Province
Alabama
ZIP/Postal Code
36607
Country
United States
Facility Name
Montgomery East Physical Therapy
City
Montgomery
State/Province
Alabama
ZIP/Postal Code
36117
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Muscle Shoals
State/Province
Alabama
ZIP/Postal Code
35674
Country
United States
Facility Name
Encore Rehabilitation
City
Phenix City
State/Province
Alabama
ZIP/Postal Code
36867
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Tuscaloosa
State/Province
Alabama
ZIP/Postal Code
35046
Country
United States
Facility Name
Cornerstone Rehabilitation
City
Batesville
State/Province
Mississippi
ZIP/Postal Code
38668
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Byram
State/Province
Mississippi
ZIP/Postal Code
39272
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Canton
State/Province
Mississippi
ZIP/Postal Code
39046
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Columbus
State/Province
Mississippi
ZIP/Postal Code
39702
Country
United States
Facility Name
Upstrem Rehabilitation
City
Forest
State/Province
Mississippi
ZIP/Postal Code
39074
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Fulton
State/Province
Mississippi
ZIP/Postal Code
38843
Country
United States
Facility Name
River City Rehabilitation
City
Greenville
State/Province
Mississippi
ZIP/Postal Code
38703
Country
United States
Facility Name
Encore Rehabilitation
City
Grenada
State/Province
Mississippi
ZIP/Postal Code
38901
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Hattiesburg
State/Province
Mississippi
ZIP/Postal Code
39402
Country
United States
Facility Name
Methodist Rehabilitation Center
City
Jackson
State/Province
Mississippi
ZIP/Postal Code
39216
Country
United States
Facility Name
Encore Rehabilitation
City
Ocean Springs
State/Province
Mississippi
ZIP/Postal Code
39564
Country
United States
Facility Name
North Sunflower Medical Center
City
Ruleville
State/Province
Mississippi
ZIP/Postal Code
38771
Country
United States
Facility Name
Cornerstone Rehabilitation
City
Southaven
State/Province
Mississippi
ZIP/Postal Code
38671
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Starkville
State/Province
Mississippi
ZIP/Postal Code
39759
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Tupelo
State/Province
Mississippi
ZIP/Postal Code
38801
Country
United States
Facility Name
Cornerstone Rehabilitation
City
Water Valley
State/Province
Mississippi
ZIP/Postal Code
38965
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Bristol
State/Province
Tennessee
ZIP/Postal Code
37620
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Cool Springs
State/Province
Tennessee
ZIP/Postal Code
37067
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Gordonsville
State/Province
Tennessee
ZIP/Postal Code
38563
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Knoxville
State/Province
Tennessee
ZIP/Postal Code
37931
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Newport
State/Province
Tennessee
ZIP/Postal Code
37821
Country
United States
Facility Name
Upstream Rehabilitation Inc.
City
Winchester
State/Province
Tennessee
ZIP/Postal Code
37398
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35906699
Citation
Tracy TF, Young HJ, Lai B, Layton B, Stokes D, Fry M, Mehta T, Riser ES, Rimmer J. Supporting successful recruitment in a randomized control trial comparing clinic and home-based exercise among adults with multiple sclerosis. Res Involv Engagem. 2022 Jul 29;8(1):35. doi: 10.1186/s40900-022-00366-6.
Results Reference
derived
PubMed Identifier
32540838
Citation
Lai B, Chiu CY, Pounds E, Tracy T, Mehta T, Young HJ, Riser E, Rimmer J. COVID-19 Modifications for Remote Teleassessment and Teletraining of a Complementary Alternative Medicine Intervention for People With Multiple Sclerosis: Protocol for a Randomized Controlled Trial. JMIR Res Protoc. 2020 Jul 3;9(7):e18415. doi: 10.2196/18415.
Results Reference
derived
PubMed Identifier
29859267
Citation
Rimmer JH, Thirumalai M, Young HJ, Pekmezi D, Tracy T, Riser E, Mehta T. Rationale and design of the tele-exercise and multiple sclerosis (TEAMS) study: A comparative effectiveness trial between a clinic- and home-based telerehabilitation intervention for adults with multiple sclerosis (MS) living in the deep south. Contemp Clin Trials. 2018 Aug;71:186-193. doi: 10.1016/j.cct.2018.05.016. Epub 2018 May 30.
Results Reference
derived

Learn more about this trial

Tele-Exercise and Multiple Sclerosis

We'll reach out to this number within 24 hrs