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Intervention group for Symptom Management (Persist Trial)
N/A
Waitlist Available
Research Sponsored by University of Oklahoma
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 8 weeks
Awards & highlights
Persist Trial Summary
This trial will assess the feasibility of using a smartphone app to help manage anxiety and depression for cancer patients receiving radiation treatments.
Eligible Conditions
- Symptom Management
- Treatment Non-Adherence
Persist Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 8 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~8 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Anxiety
Persist Trial Design
2Treatment groups
Experimental Treatment
Group I: Intervention groupExperimental Treatment1 Intervention
Intervention group will receive same measures and interventions as the assessment only group AND will receive messaging that is tailored to patient responses on EMAs. When participants provide a pattern of responses that are suggestive of heightened emotional distress, they will receive feedback and/or a prompt to complete one of the self-management exercise. The app will prompt participants to complete a brief educational video on relaxation strategies and guided relaxation exercises. Participants will have access to: 1) a "Help me Cope" button in the app that contains links to evidenced-based self-management techniques, and 2) a "Contact Counselor" button that will send a secure email to a study psychologist requesting a call. Participants will receive a coping focused message at the completion of the "Report Distress" EMAs. Participants can access these on demand intervention components and review them at any time in addition to receiving the tailored intervention messages.
Group II: Assessment only groupExperimental Treatment1 Intervention
Standard care + Daily ecological momentary assessments (EMAs)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Assessment only group
2020
N/A
~60
Intervention group
2016
N/A
~4530
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Who is running the clinical trial?
University of OklahomaLead Sponsor
455 Previous Clinical Trials
97,553 Total Patients Enrolled
Frequently Asked Questions
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