Status:
COMPLETED
Preliminary Efficacy of a One-Session Mindfulness Telehealth Intervention for Loneliness
Lead Sponsor:
University of Texas at Austin
Conditions:
Loneliness
Eligibility:
All Genders
18-70 years
Phase:
NA
Brief Summary
The primary aim of this study is to examine the efficacy of a one-session, hour-long HIPAA-compliant video platform-based mindfulness + compassion telehealth intervention on reducing feelings of lonel...
Detailed Description
Individuals are currently living in an unprecedented time where they are isolated in their homes for an extended period due to the ongoing coronavirus disease 2019 (COVID-19) pandemic. Feelings of lon...
Eligibility Criteria
Inclusion
- Access to the Internet with teleconferencing for the HIPAA-compliant video platform
- Fluent in English
- Aged 18 - 70 years old
- Currently isolating due to COVID-19
- Endorses loneliness as being among the top three issues impacting their life
- Demonstrates understanding of the constraints of the intervention (e.g. that it is a single session mindfulness training intervention focused on loneliness).
- Has access to a private setting for completing the intervention
- Denies suicidality
Exclusion
- Trauma as a primary concern
- Significant depression with depression as a primary concern
- Severe mental illness (e.g. bipolar, schizophrenia, borderline personality disorder)
Key Trial Info
Start Date :
May 25 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 26 2021
Estimated Enrollment :
91 Patients enrolled
Trial Details
Trial ID
NCT04414826
Start Date
May 25 2020
End Date
November 26 2021
Last Update
June 1 2022
Active Locations (1)
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1
Laboratory for the Study of Anxiety Disorders, University of Texas at Austin
Austin, Texas, United States, 78712