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Initial Low dose for Stress

N/A
Waitlist Available
Led By Doug Delahanty, PhD
Research Sponsored by Kent State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Inclusion Criteria: Active Medical Personnel or First-Responders working during the COVID-19 Pandemic -
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 40 weeks
Awards & highlights
No Placebo-Only Group

Summary

This trial is testing a toolkit of 3 activities to help with psychological resilience in medical personnel and first responders.

Eligible Conditions
  • Stress

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~40 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 40 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Affective Experience
Patient Health Questionnaire - 4
Treatment Acceptability Questionnaire
+1 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Active Control
Group I: Initial Low doseActive Control1 Intervention
Participants will receive only one daily positive emotion prompt in the first seven days of the toolkit use.
Group II: Initial high doseActive Control1 Intervention
Participants will receive two daily positive emotion prompts in the first seven days of use.

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Who is running the clinical trial?

Kent State UniversityLead Sponsor
43 Previous Clinical Trials
5,889 Total Patients Enrolled
Doug Delahanty, PhDPrincipal InvestigatorKent State University
John Gunstad, PhDPrincipal InvestigatorKent State University
1 Previous Clinical Trials
200 Total Patients Enrolled
~182 spots leftby Nov 2025
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