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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorThe Hong Kong Polytechnic University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Lived experience participants

Aged 18 years or older;

Have experienced suicidal thoughts and/or behaviors;

Able to read and communicate in Chinese; Professionals

Disqualifiers

Unable to provide informed consent or participate in study activities;

Currently experiencing acute suicide risk requiring immediate intervention;

Severe cognitive impairment or active psychotic symptoms that would prevent participation.

Trial design

Design model

Single group

Treatments tested in this trial

  • Digital ACT Intervention

    Behavioral

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

Treatment groups

80 Participants
are divided into 1 treatment group
Group A: Digital ACT InterventionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Intervention completion rate

The intervention completion rate will be assessed as the percentage of participants who complete the digital intervention, based on intervention usage records.

Time frame
End of the intervention (approximately 2 weeks)
2

Retention rate

The participant retention rate will be assessed as the percentage of participants who complete the post-intervention assessment and the follow-up assessment.

Time frame
End of the 1-month follow-up
3

Acceptability outcome

Acceptability of the intervention will be assessed using participant-reported ratings and feedback regarding satisfaction and overall experience with the intervention.

Time frame
End of the intervention (approximately 2 weeks)
4

Usability outcome

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.

Time frame
End of the intervention (approximately 2 weeks)

Secondary outcomes

1

Suicide ideation

Suicidal 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.

Time frame
Baseline, end of the 2-week intervention, and 1-month follow-up
2

Psychological flexibility and inflexibility

Psychological 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.

Time frame
Baseline, end of the 2-week intervention, and 1-month follow-up
3

Psychological Distress

Psychological 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.

Time frame
Baseline, end of the 2-week intervention, and 1-month follow-up
4

Mental well-being

Mental 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.

Time frame
Baseline, end of the 2-week intervention, and 1-month follow-up

Other outcomes

1

Qualitative Feedback and Design Recommendations

Qualitative feedback related to user needs, preferences, barriers, facilitators, cultural considerations, and recommendations for intervention refinement will be identified from co-design activities and feedback sessions.

Time frame
Through study completion, an average of 6 months
2

Cultural Relevance

Cultural relevance of the intervention will be assessed through participant feedback regarding the appropriateness, relevance, and cultural fit of the intervention content and delivery.

Time frame
Through study completion, an average of 6 months

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: