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Clinical Trials/NCT04346082
NCT04346082
Withdrawn
Not Applicable

Feasibility and Acceptability of Online Based Mindfulness Interventions to Relieve Distress During COVID-19 Outbreak in a Chinese Population: a Proof-of-concept Trial

Chinese University of Hong Kong1 site in 1 countryAugust 1, 2020
ConditionsStress

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stress
Sponsor
Chinese University of Hong Kong
Locations
1
Primary Endpoint
rate of recruitment
Status
Withdrawn
Last Updated
4 years ago

Overview

Brief Summary

The investigators had designed weekly mindfulness sessions (details see intervention below), which is free-of-charge and will be made available to general public who feel distressed during the outbreak of COVID-19. Face-to-face delivery of mindfulness interventions was not possible due to mandatory quarantine. The investigators hypothesize that this intervention is feasible and acceptable by the participants. As secondary outcomes, the investigators also hypothesize that the intervention can reduce stress, depressive and anxiety symptoms and enhance participants' sense of coherence

This will be a quasi-experimental study. Participants will be invited to fill in an online informed consent and questionnaire around 2 days before each mindfulness online session and another set of questionnaire immediately after each session (see outcome measures). Participants will be identified by their e-mail and therefore serial data could be obtained.

Registry
clinicaltrials.gov
Start Date
August 1, 2020
End Date
July 30, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lee Kam Pui

Clinical Assistant Professor

Chinese University of Hong Kong

Eligibility Criteria

Inclusion Criteria

  • at least 18 years of old,
  • able to speak and communicate in Cantonese
  • can read Chinese or English (because they will be asked to fill in an online questionnaire).

Exclusion Criteria

  • actively suicidal,
  • currently abusing restricted psychoactive substances
  • diagnosed to have an active psychotic disorder and self-reported active psychotic symptoms (including schizophrenia, bipolar disorder and dementia).

Outcomes

Primary Outcomes

rate of recruitment

Time Frame: from recruitment to end of study, up to 1 year

the rate of recruitment to recruit participants

rate of attendence

Time Frame: from recruitment to end of study, up to 1 year

the number of attendance to the mindfulness online group

Secondary Outcomes

  • Depression, Anxiety and Stress Scale (DASS-21)(on recruitment, after each online mindfulness sessions (weekly) until end of study, up to 1 year)
  • Sense of Coherence Scale(on recruitment, after each online mindfulness sessions (weekly) until end of study, up to 1 year)

Study Sites (1)

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