NCT06941233 · Susan Magasi
Our Peers - Empowerment and Navigational Support - Community Living (OP-ENS-CL): A Peer Navigator Intervention for Adults With Acquired Physical Disabilities
(OP-ENS-CL)
What this study is about
The goal of this clinical trial is to learn if a remote peer navigator intervention (OP-ENS - CL) for people with newly acquired physical disabilities returning to community living after rehabilitation improves self-reported social support, health, and community participation.
View original scientific description
The goal of this clinical trial is to learn if a remote peer navigator intervention (OP-ENS - CL) for people with newly acquired physical disabilities returning to community living after rehabilitation improves self-reported social support, health, and community participation.
Interventions
BEHAVIORAL
Our Peers - Empowerment and Navigational Support - Community Living (OP-ENS - CL)
Op-ENS - CL is a 12-month, remote delivered peer navigator intervention. Participants will meet with a trained peer navigator who mentors nad supports them through a manualized process of collaborative conversations, barrier identification, asset mapping, goal setting, and action planning along with on-going social support and information sharing.
Primary outcome measures
Patient Activation Measure
Time frame: Baseline, 6 months, 13 months.
The 13-item self-report measure assesses perceived knowledge, skills, and confidence for self-management
PROMIS Self-Efficacy Short Form
Time frame: Baseline, 6 months, 13 months.
4-item self-report short form measure assessing confidence in one's ability to perform specific tasks or behaviors
PROMIS Emotional Support, short form
Time frame: Baseline, 6 months, 13 months.
8-item self-report short forms assessing the availability of 3 types of emotional support
PROMIS informational support, short form
Time frame: Baseline, 6 months, 13 months.
8-item self-report short forms assessing the availability of informational support
PROMIS Instrumental Support, short form
Time frame: Baseline, 6 months, 13 months.
8-item self-report short forms assessing the availability of instrumental support
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- 1) Self-identify as a person with physical disability due to a neurological condition, including SCI, stroke, TBI, multiple sclerosis, or Parkinson's disease (according to the American Community Survey 6-Items), 2) onset of disability within the last 6 months, 3) transitioned to community living in the past 4 months, 4) able to speak, read and understand English, 5) own or have regular access to either a smartphone (Android or iOS operating system), tablet, laptop, or desktop computer with internet access. 6) adults 18 years of age or older, 7) able to provide informed consent.
Exclusion criteria
- 1) Cognitive, sensory, or physical functional limitations that interfere with effective use of the OP-ENS - CL app.
Where
- Chicago, Illinois
Collaborators
Northwestern University, Shirley Ryan AbilityLab
Related conditions & keywords
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Aug 21, 2026 · Source of record for eligibility and locations