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SCI-Lynx Mobile App for Spinal Cord Injury
N/A
Recruiting
Led By Thomas Storer, PhD
Research Sponsored by Brigham and Women's Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up follow-up assessments (1 month after randomization)
Awards & highlights
Study Summary
This trial is looking at how an online app can help people with spinal cord injury stay active and connected.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ follow-up assessments (1 month after randomization)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~follow-up assessments (1 month after randomization)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Acceptability and Usability
Secondary outcome measures
Adherence
Modified Sallis Social Support for Exercise Survey
National Institutes of Health and Northwestern University Toolbox Item Bank version 2.0- Loneliness (Aged 18+)- Fixed Form
+2 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention GroupExperimental Treatment1 Intervention
25 individuals will be randomized into the intervention group and download SCI-Lynx Mobile Application.
Group II: Control GroupActive Control1 Intervention
25 individuals will be randomized into the control group or usual care. They will then have an opportunity at the end of the 1-month to download the SCI-Lynx Mobile Application.
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Who is running the clinical trial?
Brigham and Women's HospitalLead Sponsor
1,615 Previous Clinical Trials
11,470,780 Total Patients Enrolled
The Craig H. Neilsen FoundationOTHER
55 Previous Clinical Trials
2,885 Total Patients Enrolled
Thomas Storer, PhDPrincipal InvestigatorMass General Brigham
1 Previous Clinical Trials
40 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have had a spinal cord injury at least 1 year ago.You primarily use a wheelchair or electric scooter to get around.
Research Study Groups:
This trial has the following groups:- Group 1: Control Group
- Group 2: Intervention Group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
What is the aggregate number of individuals included in this experiment?
"Correct. Clinicaltrials.gov attests that, having been placed on the website on June 14th 2023 and edited most recently on June 17th 2023, this trial is currently enrolling participants; 50 volunteers are required from 1 centre."
Answered by AI
Are any new participants being accepted for this clinical trial at present?
"Confirmed. According to the clinicaltrials.gov page, this research project which was posted on June 14th 2023 is still accepting participants. A total of 50 individuals are sought from a single medical facility for inclusion in this trial."
Answered by AI
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