Multiple Sclerosis (MS) Clinical Trials

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A Randomized Controlled Trial of a Walking Meditation Intervention (iWalk) to Enhance Resilience in Adults

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study is a randomized controlled trial of the walking meditation intervention (iWalk) program, a multi-component intervention integrating walking meditation, education, and group sessions designed to enhance resilience in individuals with multiple sclerosis (MS). The objectives are to evaluate: 1. Recruitment capability and retention rates, 2. Acceptability and adherence to the intervention, 3. Feasibility of assessment procedures, and 4. Preliminary effects on psychological, physiological, and behavioral outcomes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 110
Healthy Volunteers: t
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• 18 years or older,

• clinical diagnosis of a neurodegenerative disease such as multiple sclerosis, Alzheimer's disease, Parkinson's disease, stroke, etc.,

• have not practiced meditation regularly (e.g., 10 mins per day) and have never attended any meditation classes or community programs,

• never received meditation training via coaching/certification/life coaching,

• have internet access,

• with no severe cognitive impairment, i.e., have a score of ≥ 21 on Modified Telephonic Interview for Cognitive Status (TICS-M),

• be able to walk with or without an assistive device (Patient determined Disease Steps score ranged from 0-6),

• are willing to be randomized to an intervention or a control group,

• are willing to wear Fitbit (a wrist smart watch) for eight weeks,

⁃ are individuals who are right-handed according to the Edinburgh Handedness Questionnaire,

⁃ are willing to participate in all assessments, including in-person testing using electroencephalography (EEG) and cognitive tests, online survey/questionnaires, and online interviews or focus group discussions,

⁃ are willing to wear a Hexoskin t-shirt, which is a heart rate variability monitor, while doing the assessments in person.

Locations
United States
Illinois
University of Illinois Urbana-Champaign
RECRUITING
Urbana
Contact Information
Primary
Chung-Yi Chiu
chiucy@illinois.edu
12172446435
Backup
Vaishnavi Sridharan
vs35@illinois.edu
Time Frame
Start Date: 2025-06-01
Estimated Completion Date: 2029-12-31
Participants
Target number of participants: 90
Treatments
Active_comparator: iWalk Program
This group receives the complete iWalk program.
Active_comparator: Education Only without Walking Mindfulness Practice
This group receives only education part of the iWalk program without walking mindfulness sessions.
No_intervention: Control Group
This group does not receive any intervention and are placed on a waiting list.
Related Therapeutic Areas
Sponsors
Leads: University of Illinois at Urbana-Champaign

This content was sourced from clinicaltrials.gov