Skip to main content
Clinical Trials/NCT04496804
NCT04496804CompletedNot Applicable

BIPAMS-Brain:Examining the Neural Effects of a Behavioral Intervention for Physical Activity in Multiple Sclerosis

University of Alabama at Birmingham1 site in 1 country24 target enrollmentStarted: November 2, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
24
Locations
1
Primary Endpoint
Minutes of moderate to vigorous physical activity - Baseline

Study Overview

Brief Summary

Multiple sclerosis [MS] is a prevalent neurological disease that is the leading cause of irreversible neurological disability among young women and the second leading cause of disability among young men in the United States. This disease results in the progressive loss of walking mobility and substantial worsening of cognition, symptoms, and quality of life over time. There is evidence that physical activity is beneficially associated with aerobic fitness and brain structure and function in persons with MS. Nevertheless, this population is strikingly sedentary and physically inactive. This highlights a vital opportunity to improve aerobic fitness and brain health by developing behavioral interventions that increase physical activity. To that end, this project is a Phase-II randomized control trial for examining the efficacy of a behavioral intervention that is based on social-cognitive theory and delivered through the Internet for increasing physical activity and, secondarily, improving aerobic fitness and brain structure and function in persons with MS.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •diagnosis of multiple sclerosis
  • •relapse free in the last 30 days
  • •being non-active defined as not engaging in regular activity (30 minutes accumulated per day) on more than 2 days of the week during the previous 6 months
  • •ambulate without assistance
  • •low risk for contraindications for MRI

Exclusion Criteria

  • •moderate or high risk for undertaking strenuous or maximal exercise

Arms & Interventions

Behavioral Intervention for Physical Activity in MS (BIPAMS)

Experimental

The current behavioral intervention consists of two primary components; an Internet website and one-on-one video chats with a behavioral coach. The Internet website involves content delivered through interactive video courses. The interactive video courses are based on elements of social cognitive theory. Each courses consists of an introduction, the primary content, and a take home message. The interactive courses include embedded, supplementary options such as videos on content and worksheets related to the topic. A pedometer is provided for tracking steps, and these steps will be entered into the website so progress can be monitored. The chats support adherence to the intervention, discussion of website material, supportive accountability, and reporting of adverse events/injuries. The chats are conducted face-to-face through Skype. The chats occur 7 times during the first 2 months, 4 times during the second 2 months, and twice during the final 2 months of the intervention.

Intervention: Behavioral Intervention for Physical Activity in MS (BIPAMS) (Behavioral)

Wellness for MS (WellMS)

Sham Comparator

Provides an Internet website and one-on-one video chats that discuss materials about self-managing multiple sclerosis (MS) consequences and health indicators through methods other than physical activity. The materials are transformations of brochures provided by the National MS Society, including Gait or Walking Problems: The Basic Facts; MS and Your Emotions; Pain: The Basic Facts; Solving Cognitive Problems; Taming Stress in MS; Food for Thought: MS and Nutrition; and Vitamins, Minerals, and Herbs: An Introduction. The delivery of the Internet materials and chat sessions will occur on the same time schedule and frequency as the intervention condition, and will have a comparable time commitment. The control condition will not involve tracking steps and a pedometer with not be provided.

Intervention: Wellness for MS (WellMS) (Behavioral)

Outcomes

Primary Outcomes

Minutes of moderate to vigorous physical activity - Baseline

Time Frame: Assessment will be conducted before the intervention

Activity monitors are Actigraph accelerometers that participants will wear on an elastic belt around their waist for 7 days. These activity monitors measure how frequently and how much an individual moves.

Minutes of moderate to vigorous physical activity - Post intervention

Time Frame: Assessment will be conducted immediately after the intervention

Activity monitors are Actigraph accelerometers that participants will wear on an elastic belt around their waist for 7 days. These activity monitors measure how frequently and how much an individual moves.

Secondary Outcomes

  • volume of subcortical grey matter brain structures - post intervention(Assessment will be conducted immediately after the intervention)
  • resting state functional brain connectivity - post intervention(Assessment will be conducted immediately after the intervention)
  • cardiorespiratory fitness; oxygen consumption during exercise - baseline(Assessment will be conducted before the intervention)
  • distance walked - baseline(Assessment will be conducted before the intervention)
  • distance walked - post-intervention(Assessment will be conducted immediately after the intervention)
  • information processing speed; cognitive function - baseline(Assessment will be conducted before the intervention)
  • volume of subcortical grey matter brain structures - baseline(Assessment will be conducted before the intervention)
  • cardiorespiratory fitness; oxygen consumption during exercise - post intervention(Assessment will be conducted immediately after the intervention)
  • information processing speed; cognitive function - post intervention(Assessment will be conducted immediately after the intervention)
  • resting state functional brain connectivity - baseline(Assessment will be conducted before the intervention)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Robert W Motl

Primary Investigator

University of Alabama at Birmingham

Study Sites (1)

Loading locations...

Similar Trials

Examining the Neural Effects of a... | Clinical Trial