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A tailored mindfulness-based intervention for people in mental health recovery: an exploratory study

Development and implementation of a mindfulness-based intervention (REMIND2.0) for people in recovery in Hong Kong: the exploratory pilot randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN13689468
Enrollment
28
Registered
2022-07-19
Start date
2020-07-01
Completion date
Unknown
Last updated
2022-08-05

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

Conditions

Facilitation of personal recovery among people with mental illness Mental and Behavioural Disorders

Interventions

After screening and giving informed consent, participants were randomly assigned to either the mindfulness-based intervention (MBI) or the relaxation training (RT). RT was designed the closely mirror

Sponsors

Hong Kong Baptist University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18 years or above 2. Permanent Hong Kong residents 3. Diagnosed with mental illness with standardised diagnostic criteria, such as the Classification of Diseases (11th ed.; ICD-11; World Health Organization, 2018) or Diagnostic and Statistical Manual of Mental Disorders (5th ed.; DSM-5; American Psychiatric Association, 2013), for any length of illness 4. Capable of providing informed consent to participate in the trial; (v) able to understand Chinese languages to engage in the intervention or to complete written assessment in Chinese; and 5. A service user from the community-based mental health service

Exclusion criteria

Exclusion criteria: 1. Established diagnosis of learning disability or major cognitive impairment arising from any underlying medical condition resulting in significant functional impairment 2. Primary diagnosis of substance abuse, as substance use may increase and/or trigger symptoms of mental illnesses, and hence it has different trajectories from other mental illnesses 3. Mental state that precludes the possibility of engaging in the intervention (e.g. significant thought disorder) 4. Engagement in concurrent mindfulness intervention 5. Do not provide informed consent 6. Refused to be randomised

Design outcomes

Primary

MeasureTime frame
1. Personal recovery: Recovery Assessment Scale (RAS-C) at pre-, post-intervention and 1-month follow-up Trait mindfulness: Kentucky Inventory of Mindfulness Skills (KIMS-17-C), Mindful Attention Awareness Scale (MAAS) at pre-, post-intervention and 1-month follow-up 2. Self-compassion: Self-compassion Scale (SCS) at pre-, post-intervention and 1-month follow-up 3. Resilience: Connor-Davidson Resilience Scale (CD-RISC) at pre-, post-intervention and 1-month follow-up 4. Mindfulness-based intervention participants' experiences and views: Qualitative Interviews at post-intervention and 1-month follow-up

Secondary

MeasureTime frame
1. Depression, Stress and Anxiety: The Depression Anxiety Stress Scales (DASS-21) at pre-, post-intervention and 1-month follow-up 2. Positive and negative affect: Positive and Negative Affect Schedule (PANAS) at pre-, post-intervention and 1-month follow-up 3. Quality of life and general health: The World Health Organization Quality of Life – BREF (WHOQOL-BREF) at pre-, post-intervention and 1-month follow-up

Countries

Hong Kong

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026