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NCT05616806
Long COVID-19 Intervention Using Digital Health & Technology
Conditions: Long COVID, Distress Tolerance
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: 1
Phase: NA
Enrollment: 10
Sponsor: Rhode Island Hospital
Location: United States
Summary
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
Eligibility Criteria
Inclusion Criteria:Must be over 18 years of ageMust speak English proficientlyMust own a text-enabled deviceDiagnosis (self-reported) of COVID-19Diagnosis (self-reported) of Long-COVID symptom(s)Must be able to provide written, informed consentExclusion Criteria:Not fluent in EnglishLimited mental capacity or inability to provide informed written consent
Source: ClinicalTrials.gov (NCT05616806). StuddyBuddy aggregates publicly available trial information.
