Long COVID-19 Intervention Using Digital Health & Technology (LIGHT)

Lifespan

Status: Not yet enrolling

Conditions: Distress Tolerance; Long COVID

Treatments: Behavioral: iENDURE

Study type: Interventional

Funder types: Other

Identifiers

NCT05616806

2022003396

Details and patient eligibility

About

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

Enrollment: 10 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Must be over 18 years of age
• Must speak English proficiently
• Must own a text-enabled device
• Diagnosis (self-reported) of COVID-19
• Diagnosis (self-reported) of Long-COVID symptom(s)
• Must be able to provide written, informed consent

Exclusion criteria

• Not fluent in English
• Limited mental capacity or inability to provide informed written consent

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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10 participants in 1 patient group

distress tolerance skills training

Experimental group

Description:

technology delivered distress tolerance skills training

Treatment:

Behavioral: iENDURE