Clinical trial Recruiting at 1 site Interventional Ages 21 to 65

Online skills training to improve emotion regulation and relationships for adults with childhood adversity and mild depression

Official title: Internet-Delivered Skills Training in Affective and Interpersonal Regulation (i-STAIR) for Individuals With Adverse Childhood Experiences and Subsyndromal Depression: A Pilot Study

Run by Institute of Mental Health, Singapore · NCT07118072 · Data updated 2026-11-12

This project will test whether an 8-week online i-STAIR program helps adults with a history of childhood adversity and subthreshold depression manage emotions and relationships to prevent worsening depression.

More Subthreshold Depression trials

Quick facts

Study typeInterventional
Ages21 Years to 65 Years
SexAll
Enrollment150 (estimated)
SponsorInstitute of Mental Health, Singapore
Academic / other
Locations1 site (Singapore)
StatusRecruiting
StartedOctober 31, 2025
Main results expectedDecember 2028
Study endsDecember 2028
Registry record updatedNovember 4, 2026
Trial IDNCT07118072 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 21–65 in Singapore who speak English, have a history of adverse childhood experiences, and screen positive for subsyndromal depression while not having a current diagnosed mental disorder or receiving DBT are ideal candidates.

Probably not a fit

People with a current diagnosable mental disorder, cognitive impairment, those currently in DBT, or pregnant women are excluded and are unlikely to benefit from this specific online prevention program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The pilot compares an 8-week internet-delivered Skills Training in Affective and Interpersonal Regulation (i-STAIR) program to online general psychoeducation in adults with adverse childhood experiences and subsyndromal depression. Participants will be assigned to one of the two online interventions and complete measures at baseline, post-intervention (8 weeks), and at a 3-month follow-up. Primary outcomes include emotion dysregulation, interpersonal skills, depressive symptoms, and PTSD symptoms. The intervention is delivered fully online to English-speaking Singapore citizens or permanent residents aged 21–65, with exclusion of those with current diagnosed mental disorders, cognitive impairment, current DBT, or pregnancy.

Why it matters

Potential benefit: If successful, the program could reduce depressive and PTSD symptoms and improve emotion regulation and interpersonal functioning, potentially preventing progression to full depressive disorder.

How similar studies have gone: STAIR-based interventions have shown benefit for emotion regulation and trauma-related symptoms in prior research, but internet-delivered i-STAIR for preventing depression in ACE-exposed adults with subthreshold depression is relatively novel with limited prior data.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Exposed to mild, moderate or severe adverse childhood experiences (ACEs)
* Screened positive for subsyndromal depression
* Singapore citizens or permanent residents (PRs)
* Aged 21 years to 65 years
* Able to speak and understand English
* Willing and able to undergo intervention and assessment online

Exclusion Criteria:

* Currently diagnosed with any mental disorder diagnoses;
* Experience cognitive impairment as determined by attending physician
* Have received or currently receiving dialectical behavior therapy (DBT) due to similarities with i-STAIR
* Female participants who are pregnant

Where it's running

  • Institute of Mental Health
    Singapore, Singapore
    Recruiting

Study contacts

  • Principal investigator: Siow Ann Chong, MD — Institute of Mental Health, Singapore
  • Study coordinator: Siow Ann Chong, MD
  • Email: imhresearch@imh.com.sg
  • Phone: +65 63892000

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.