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Trial record 1 of 1 for:    flexibility toning balance multiple sclerosis
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FlexToBa for People With Multiple Sclerosis

This study has been completed.
Sponsor:
Collaborator:
National Multiple Sclerosis Society
Information provided by (Responsible Party):
Edward McAuley, University of Illinois at Urbana-Champaign
ClinicalTrials.gov Identifier:
NCT01993095
First received: October 18, 2013
Last updated: February 21, 2017
Last verified: February 2017
  Purpose
The purpose of this study is to test the effectiveness of a DVD-delivered, home-based six-month physical activity intervention for people with Multiple Sclerosis.

Condition Intervention
Multiple Sclerosis Behavioral: Home-based, DVD-delivered physical activity Behavioral: Behavioral: Usual care/Wait list

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Improving Functional Performance in Persons With MS Via Physical Activity DVD Intervention

Resource links provided by NLM:


Further study details as provided by Edward McAuley, University of Illinois at Urbana-Champaign:

Primary Outcome Measures:
  • Change from baseline to six-months in assessments of functional fitness of sedentary adults who have Multiple Sclerosis [ Time Frame: Baseline and six months ]

    The measurements will include:

    Short physical performance battery -- measures walking speed, ability to rise from a chair, and standing balance


  • Change from baseline to six-months in assessments of functional fitness of sedentary adults who have MS [ Time Frame: Baseline and six-months ]

    Measurements will include:

    Timed 20-foot walk test -- walk 25 feet as quickly as possible;


  • Change in assessments of functional fitness assessments in sedentary adults with MS [ Time Frame: Baseline and six-months ]

    Measurements will include:

    6-minute walk test -- walk as much as possible (in terms of distance) for 6 minutes;


  • Change from baseline to six-months in assessments of functional fitness of sedentary adults with MS [ Time Frame: Baseline and six-months ]

    Measurements will include:

    Grip strength -- using a dynamometer, participants will demonstrate isometric grip strength;


  • Change from baseline to six-months in assessments of functional fitness of sedentary adults who have MS [ Time Frame: Baseline and six-months ]

    Measurements will include:

    Flexibility -- sit and reach (lower body flexibility) and back scratch test (upper body flexibility)


  • Change from baseline to six-months in assessments of functional fitness of sedentary adults with MS [ Time Frame: Baseline and six-months ]

    Measurements will include:

    Upper body strength -- bicep curls consisting of lifting a light hand-weight as many times as possible in 30-seconds;


  • Change from baseline to six-months in assessments of functional fitness of sedentary adults who have MS [ Time Frame: Baseline and six-months ]

    Measurements will include:

    Balance -- a timed (up to 30-seconds) unassisted one-leg stand test with eyes open on each leg.


  • Change from baseline to six-months in assessments of reported quality of life in people with MS [ Time Frame: Baseline and six months ]
    The Leeds Multiple Sclerosis Quality of Life Scale will be used as a disease specific quality of life measure for people with MS.

  • Change from baseline to six-months in assessments of reported quality of life in people with MS [ Time Frame: Baseline and six-months ]
    The Satisfaction with Life Scale will be used to assess global life satisfaction and is sensitive enough to detect changes in participants' perceptions over the course of a clinical intervention.


Secondary Outcome Measures:
  • Change from baseline to six-months in assessments of cognitive performance in sedentary adults with MS [ Time Frame: Baseline and six months ]
    The Brief International Cognitive Assessment for Multiple Sclerosis (BICAMS) battery, which will be administered to assess cognitive performance.

  • Change from baseline to six-months in assessments of reported barriers self-efficacy in people with MS [ Time Frame: Baseline and six months ]
    Participants' situation-specific self-confidence for physical activity will be assessed using The Barriers Self-Efficacy Scale, which taps subjects' perceived capabilities to exercise three times per week for 40 minutes over the next two months in the face of commonly identified barriers to participation.

  • Changes in physical activity relating to specified exercise program in sedentary adults with MS [ Time Frame: Baseline and six months ]
    Adherence to exercise program as documented by daily exercise logs.

  • Objective changes in physical activity in sedentary adults with MS [ Time Frame: Baseline and six months ]
    Objective assessment of physical activity via accelerometry over seven days time.

  • Self-reported changes in physical activity in sedentary adults with MS [ Time Frame: Baseline and six months ]
    Subjective assessment of physical activity via the Godin Leisure Time Exercise Questionnaire, which assesses frequency of involvement in strenuous, moderate and light activities.

  • Change from baseline to six-months in assessments of reported gait self-efficacy in sedentary adults with MS [ Time Frame: Baseline and six-months ]
    Participants' situation-specific self-confidence for physical activity will be assessed using The Gait Self-Efficacy Scale, which will assess participants' beliefs in their capabilities to negotiate stairs and objects in their path.

  • Change from baseline to six-months in assessments of reported exercise self-efficacy in sedentary people with MS [ Time Frame: Baseline and six-months ]
    The Exercise Self-Efficacy Scale will assess participants' beliefs in their ability to continue exercising on a three time per week basis at moderate intensities for 40+ minutes per session in the future.

  • Change from baseline to six-months in assessments of reported self-efficacy of walking in sedentary people with MS [ Time Frame: Baseline and six-months ]
    Walking Self-Efficacy Scale for Duration will assess participants' beliefs in their physical capability to successfully complete incremental 5-minute intervals (up to 40 minutes)of walking at a moderately fast pace.


Enrollment: 50
Study Start Date: October 2013
Study Completion Date: September 2014
Primary Completion Date: September 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Experimental: FlexToBa physical activity DVD
Participants in this arm will receive a physical activity program delivered by DVD that focuses on exercises targeting flexibility, toning and balance. These exercises will be progressive in nature throughout the six months and will also focus on modifications for all ability levels. Participants will be provided with three DVDs including: an Introduction to physical activity, Sessions 1-3, and Sessions 4-6, which they will be asked to watch and participate in over the course of six months.
Behavioral: Home-based, DVD-delivered physical activity
Subjects will be participating in a home-based physical activity program that focuses on flexibility, toning and balance. Exercises will be progressive over the six-months and will highlight modifications for varying levels. This program will be delivered on 3 DVDs. Participants will be asked to exercise with the DVD at least three times per week.
Active Comparator: Usual care-Wait list
Participants in this arm will receive a DVD that focuses on healthy aging topics but does not include physical activity. They will receive the FlexToBa DVD after the completion of the 6-month follow-up testing.
Behavioral: Behavioral: Usual care/Wait list
Participants in this arm will receive a DVD that focuses on healthy aging topics but does not include physical activity. They will receive the FlexToBa DVD after the completion of the 6-month follow-up testing.

Detailed Description:
Persons with MS are less likely to be active than their healthy counterparts, a statistic that is compounded by the symptom manifestations of MS. However, there is increasing evidence to support the importance of physical activity in MS. Unfortunately, structured, safe, and efficacious physical activity programs that are often conducted in medical or university settings are often not accessible to many older adults with or without MS. We propose to conduct a randomized controlled pilot trial testing the efficacy of a DVD-delivered physical activity intervention which targets factors that have the potential to reduce disability in older adults with MS. This DVD-based intervention has been previously approved by the IRB at the University of Illinois for a similar study with low-active, community-dwelling older adults (IRB Protocol Number: 09765). This novel intervention provides systematic, programmatic activities with alternative versions of each exercise that allow individuals of all capabilities to complete the program successfully. It focuses on improving flexibility, strength, and balance and has been demonstrated to be feasible, well-accepted, and efficacious in a large sample of older adults without MS. Importantly, intervention resulted in clinically significant improvements in the Short Physical Performance Battery, reliable determinant of disability, institutionalization, morbidity, and mortality. If such an intervention was equally successful in older persons with MS, this could have considerable public health impact.
  Eligibility

Ages Eligible for Study:   50 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • being non-active, defined as reporting not engaging in regular activity (30 minutes accumulated per day) on more than two days of the week in the prior six months;
  • aged 50 years and older;
  • fluent in English;
  • relapse-free in the last 30 days;
  • ambulatory with minimal assistance(i.e., walk independently or with a single-point assistive walking device such as a cane);
  • the provision of medical clearance for participation in a physical activity program by participants' physicians, along with a physician-confirmed diagnosis of MS (communication with physicians will be facilitated by research staff).

Exclusion Criteria:

  • self-reported physical activity on a regular basis within the last six months (2 times or more per week);
  • younger than 50 years of age;
  • relapse in the last 30 days;
  • no regular access to a television;
  • no physician-confirmed diagnosis of multiple sclerosis;
  • unable to successfully score above 21 (out of 39)on the Telephone Interview of Cognitive Status questionnaire (TICS-M).
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01993095

Locations
United States, Illinois
University of Illinois at Urbana-Champaign
Urbana, Illinois, United States, 61801
Sponsors and Collaborators
University of Illinois at Urbana-Champaign
National Multiple Sclerosis Society
Investigators
Principal Investigator: Edward McAuley, PhD University of Illinois at Urbana-Champaign
  More Information

Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Edward McAuley, Professor, Kinesiology and Community Health, University of Illinois at Urbana-Champaign
ClinicalTrials.gov Identifier: NCT01993095     History of Changes
Other Study ID Numbers: IL-0009
Study First Received: October 18, 2013
Last Updated: February 21, 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Keywords provided by Edward McAuley, University of Illinois at Urbana-Champaign:
Multiple Sclerosis
Quality of Life
Functional Fitness

Additional relevant MeSH terms:
Sclerosis
Multiple Sclerosis
Pathologic Processes
Demyelinating Autoimmune Diseases, CNS
Autoimmune Diseases of the Nervous System
Nervous System Diseases
Demyelinating Diseases
Autoimmune Diseases
Immune System Diseases

ClinicalTrials.gov processed this record on September 19, 2017