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Development of a Digital Acceptance and Commitment Therapy Intervention for Suicide Prevention in Adults Through Co-design

Development of a Digital Acceptance and Commitment Therapy Intervention for Suicide Prevention in Adults Through Co-design

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07733596
Enrollment
80
Registered
2026-07-29
Start date
2026-07-15
Completion date
2026-12-30
Last updated
2026-07-29

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

Conditions

Co-design, Suicide, Suicide Prevention

Brief summary

Suicide is a major public health concern and there is a need for accessible and scalable interventions to support individuals experiencing suicidal thoughts. The aim of this study is to develop a digital Acceptance and Commitment Therapy (ACT) intervention for suicide prevention in Chinese adults through co-design. The study will involve literature review, interviews, and co-design activities to identify user needs, preferences, and contextual factors, and to develop the intervention. Following intervention development, a pilot study will be conducted to evaluate the feasibility, usability, acceptability, and user engagement of the intervention. Findings from this study will inform further refinement of the intervention and future evaluation studies.

Interventions

BEHAVIORALDigital ACT Intervention

A co-designed digital Acceptance and Commitment Therapy (ACT) intervention for suicide prevention

Sponsors

The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* Inclusion Criteria Lived experience participants 1. Aged 18 years or older; 2. Have experienced suicidal thoughts and/or behaviors; 3. Able to read and communicate in Chinese; Professionals <!-- --> 1. Aged 18 years or older; 2. Professionals with experience relevant to suicide prevention, Acceptance and Commitment Therapy (ACT), digital mental health, or related fields; *

Exclusion criteria

1. Unable to provide informed consent or participate in study activities; 2. Currently experiencing acute suicide risk requiring immediate intervention; 3. Severe cognitive impairment or active psychotic symptoms that would prevent participation.

Design outcomes

Primary

MeasureTime frameDescription
Intervention completion rateEnd of the intervention (approximately 2 weeks)The intervention completion rate will be assessed as the percentage of participants who complete the digital intervention, based on intervention usage records.
Retention rateEnd of the 1-month follow-upThe participant retention rate will be assessed as the percentage of participants who complete the post-intervention assessment and the follow-up assessment.
Acceptability outcomeEnd of the intervention (approximately 2 weeks)Acceptability of the intervention will be assessed using participant-reported ratings and feedback regarding satisfaction and overall experience with the intervention.
Usability outcomeEnd of the intervention (approximately 2 weeks)Usability will be assessed using the System Usability Scale (SUS), a 10-item self-report questionnaire. Total scores range from 0 to 100, with higher scores indicating better usability of the intervention.

Secondary

MeasureTime frameDescription
Suicide ideationBaseline, end of the 2-week intervention, and 1-month follow-upSuicidal ideation will be assessed using the Beck Scale for Suicide Ideation (BSSI). Each item is rated on a 3-point scale ranging from 0 to 2, with higher scores indicating greater suicidal ideation.
Psychological flexibility and inflexibilityBaseline, end of the 2-week intervention, and 1-month follow-upPsychological flexibility and inflexibility will be assessed using the Multidimensional Psychological Flexibility Inventory-24 (MPFI-24). Each item is rated on a 6-point scale ranging from 1 to 6. Higher scores on the flexibility and inflexibility subscales indicate greater psychological flexibility and psychological inflexibility, respectively.
Psychological DistressBaseline, end of the 2-week intervention, and 1-month follow-upPsychological distress will be assessed using the Depression Anxiety Stress Scales (DASS). Each item is rated on a 4-point scale ranging from 0 to 3, with higher scores indicating greater psychological distress.
Mental well-beingBaseline, end of the 2-week intervention, and 1-month follow-upMental well-being will be assessed using the Mental Health Continuum-Short Form (MHC-SF). Each item is rated on a 6-point scale ranging from 0 to 5, with higher scores indicating greater mental well-being.

Countries

China

Contacts

CONTACTTao Zhang
tao-t.zhang@connect.polyu.hk+85294233827
PRINCIPAL_INVESTIGATORTao Zhang

The Hong Kong Polytechnic University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 30, 2026