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Feasibility of Online Based Mindfulness Interventions During COVID-19 Outbreak

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

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04346082
Enrollment
0
Registered
2020-04-15
Start date
2020-08-01
Completion date
2021-07-30
Last updated
2021-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress

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.

Interventions

BEHAVIORALonline mindfulness group

Each weekly mindfulness session will last 45 to 60 minutes and will be held on an online platform (e.g. Zoom) via a livestream video. It will consist of short mindfulness exercise(s) of 10-30 minutes, including mindful tasting, mindful stretching, mindful walking, and body scan followed by group discussion to share, explore and make sense of the meditative experience. The intervention will be held in Cantonese.

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

participants receiving online mindfulness session(s)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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).

Design outcomes

Primary

MeasureTime frameDescription
rate of recruitmentfrom recruitment to end of study, up to 1 yearthe rate of recruitment to recruit participants
rate of attendencefrom recruitment to end of study, up to 1 yearthe number of attendance to the mindfulness online group

Secondary

MeasureTime frameDescription
Depression, Anxiety and Stress Scale (DASS-21)on recruitment, after each online mindfulness sessions (weekly) until end of study, up to 1 yearDepression, anxiety and stress will be measured using the Depression, Anxiety and Stress Scale (DASS-21), which was validated in Chinese population with high internal consistency. The 21-item DASS-21 has three subscales designed to measure depression, anxiety and stress, with each subscale containing 7 items. Participants are required to rate each statement in DASS-21 using a 4-point Likert scale from did not apply to me at all to applied to me very much or most of the time in the prior one week. Higher scores represent higher level of psychological distress.
Sense of Coherence Scaleon recruitment, after each online mindfulness sessions (weekly) until end of study, up to 1 yearSense of Coherence (SOC) will be assessed by the 13-item Sense of Coherence Scale (SOC-13) based on Antonovsky (1987)'s measurement of the comprehensibility, manageability, and meaningfulness of a person's life events . Participants will rate each statement in SOC-13 on a 7-point Likert scale from very often to very seldom or never. SOC-13 has been validated in Chinese population with high internal consistency. The higher the score, the higher the sense of coherence

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026