Feasibility Study of Single-session Solution Focused Consultation to Enhance Treatment Engagement

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-99
SponsorNanyang Technological University

About this trial

This research aims to explore whether a single-session solution-focused consultation (SSC) can increase mental health service engagement among patients with comorbid chronic physical diseases and mental health problems (CPDMHP).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

A history of one or more chronic physical diseases based on the Ministry of Health (Singapore) Chronic Disease Management Programme guidelines; 2. A score of 5 or more on the Patient Health Questionnaire (PHQ-9) or Generalized Anxiety Disorder-7 (GAD-7); 3. Not currently engaged in formal mental health service; 4. Conversant in the English language; 5. Receiving treatment in a community healthcare setting

Disqualifiers

A history of psychosis, intellectual disability, or pervasive developmental disorders

Trial design

Design model

Parallel

Treatments tested in this trial

  • Single-session solution focused consultation

    Behavioral

    In the SSC, the interventionist first sets expectations, explaining that the session is a means of providing short-term support. The interventionist will then praise the participant for agreeing to receive support and introduce the Action Plan, which will guide the session's structure. The interventionist will then work with the participant to (1) identify a specific, modifiable issue they are facing; (2) use the "miracle question" to envision their ideal outcome where the problem is resolved, and rates their current proximity to that; (3) determine the "smallest possible step" they can take towards this outcome through a scaling exercise; and (4) develop a personalized action plan that leverage on their current resources to begin addressing the problem. Upon ending the SSC, the interventionist writes a personalized note to the participant, highlighting their strengths and expressing confidence in their ability to follow through.

  • Single-session supportive intervention

    Behavioral

    In the supportive consultation session, the interventionist will allow the participant to decide what they wish to discuss during the session and listen empathetically, validate their feelings and offer reassurance to the patient. The exact wording or questions will vary depending on the client's needs and sharing.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Active Control GroupActive comparator 1 intervention
Group B: Intervention GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Treatment Engagement - Uptake

Endorsement of interest in referral for mental health services or follow-up session with interventionist

Time frame
Post-intervention (immediate)
2

Treatment engagement - Attendance

Attendance at intake session for mental health services or follow-up session with interventionist

Time frame
2-weeks post-intervention
3

Feasibility - Intervention Completion Rate

Completion of intervention action plans

Time frame
Post-intervention (immediate)
4

Acceptability - Usefulness of intervention

Single item measure on helpfulness of consultation in addressing concern/s

Time frame
Post-intervention (immediate)

Secondary outcomes

1

Perceived agency

State Hope Scale (SHS) - Pathways Subscale

Time frame
From baseline to post-intervention (immediate)
2

Hope

Beck's Hopelessness Scale (BHS-4)

Time frame
From baseline to post-intervention (immediate) and two-week post intervention

Other outcomes

1

Depression

Patient's Health Questionnaire (PHQ-9)

Time frame
From baseline to two-weeks post intervention
2

Anxiety

Generalized Anxiety Disorder (GAD-7)

Time frame
From baseline to two-weeks post intervention
3

Change readiness

Readiness Ruler

Time frame
From baseline to post-intervention (immediate) and two-week post intervention
4

Life satisfaction

Single-item measuring satisfaction with life

Time frame
From baseline to two-week post intervention

Sponsors and contacts

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

Nanyang Technological University

Lead sponsor

National Medical Research Council (NMRC), Singapore

Collaborator