10 Participants Needed

Digital Health Program for Post-COVID Syndrome

(LIGHT Trial)

Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Rhode Island Hospital
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

Trial Summary

What is the purpose of this trial?

The current study seeks to pilot test the iENDURE (Enhancing Distress tolerance to Uplift motivation in Recovery) intervention among 10 participants with Long COVID (Coronavirus Disease) symptoms. Following informed consent procedures, participants will complete a brief baseline assessment of self-report measures. Participants will then engage in the iENDURE intervention (described below) for 4 weeks. At the end of the intervention period, participants will complete another brief assessment of self-report measures and a qualitative interview about their experience with the program. Participants will be compensated for completing the baseline and post-intervention assessments

Research Team

KL

Kirsten Langdon, PhD

Principal Investigator

Brown University

Eligibility Criteria

This trial is for adults over 18 who have self-reported Long COVID symptoms and a past diagnosis of COVID-19. Participants must own a device capable of texting and speak English well enough to give informed consent.

Inclusion Criteria

Must own a text-enabled device
I have symptoms of Long-COVID.
I have been diagnosed with COVID-19.
See 2 more

Exclusion Criteria

I am not fluent in English.
I am unable to understand or sign the consent form due to mental capacity.

Timeline

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Treatment

Participants engage in the iENDURE intervention for Long COVID symptoms

4 weeks
Weekly virtual sessions

Follow-up

Participants complete a post-intervention assessment and qualitative interview

1 week

Treatment Details

Interventions

  • iENDURE
Trial Overview The iENDURE program, aimed at improving distress tolerance in individuals with Long COVID, is being tested. It involves a baseline assessment, a 4-week intervention period using digital health technology, followed by another assessment and interview.
Participant Groups
1Treatment groups
Experimental Treatment
Group I: distress tolerance skills trainingExperimental Treatment1 Intervention
technology delivered distress tolerance skills training

Find a Clinic Near You

Who Is Running the Clinical Trial?

Rhode Island Hospital

Lead Sponsor

Trials
275
Recruited
71,400+

Brown University

Collaborator

Trials
480
Recruited
724,000+
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