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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 three months
Awards & highlights
PSC Trial Summary
This trial develops an 8-session group intervention over 2-3 months to help people reframe their sense of self and find purpose after significant life events. It aims to improve psychological well-being, engagement in everyday activities, and purpose in life.
PSC Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ three months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~three months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Purpose in Life
PSC Trial Design
1Treatment groups
Experimental Treatment
Group I: Compass CourseExperimental Treatment1 Intervention
Four groups of up to 12 participants (48 total) will receive the study intervention during Spring and Fall 2022. All participants will complete study questionnaires before and after the sessions.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Compass Course
2018
N/A
~70
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Who is running the clinical trial?
Mary RadomskiLead Sponsor
2 Previous Clinical Trials
320 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You are willing to install and utilize a mobile application on your personal device, in order to receive prompts from the study team.You are proficient in English.You are unable to see, hear, or speak, even with the help of devices.You possess an electronic mail address.You possess a device (computer with webcam or tablet) capable of using Zoom during sessions.You are 18 years of age or older.You commit to attending all group meetings, responding regularly to notifications, and devoting half an hour each week to completing assignments.You have obtained medical-rehabilitative care for persistent concussion symptoms in the past year as evidenced by documentation within EPIC (e.g., ICD9 or ICD10 codes) or a clinician referral to the study.You have the requisite technology and internet access to engage in virtual conferencing.You have access to a wired or wireless broadband connection (3G, 4G/LTE).You possess a smartphone with either iOS 9.0 - 9.3, 10.0 - 10.3, 12, 13.3, 13.7, 14.0 - 14.4 or later versions of Apple's operating system; or Android 8.0 - 8You have experienced persisting concussion symptoms for at least 3 months following a head injury sustained within the past two years.
Research Study Groups:
This trial has the following groups:- Group 1: Compass Course
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.
Concussion Patient Testimony for trial: Trial Name: NCT05780658 — N/A
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