NCT07851792

Brief Summary

The goal of this non-randomized trial is to partially digitalize and develop a web-based resilience-building intervention and pilot-test its feasibility, acceptability, and appropriateness in an undergraduate sample over a 6-month implementation period. The main questions it aims to answer are:

  • What are the rates of recruitment, adoption, and full program completion?
  • What is the intervention's overall effectiveness in enhancing resilience and mental health outcomes? Researchers will compare the partially digitalized intervention with a structurally equivalent in-person mode of delivery.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
400

participants targeted

Target at P75+ for not_applicable

Timeline
8mo left

Started Nov 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 17, 2026

Completed
3 months until next milestone

First Posted

Study publicly available on registry

October 1, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

November 1, 2026

Expected
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2027

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2027

Last Updated

October 1, 2026

Status Verified

September 1, 2026

Enrollment Period

8 months

First QC Date

July 17, 2026

Last Update Submit

September 25, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Feasibility of the digitalized individual components

    Proportion of eligible individuals who consent, participate, and complete the intervention

    From baseline to end of intervention at 6 weeks

  • Acceptability of the digitalized individual components

    Quantitative measure of participant satisfaction based on a 5-point Likert scale ranging from "1=Very Dissatisfied" to "5=Very Satisfied," and qualitative description of participants' perspectives on acceptability of the intervention.

    From baseline to end of intervention at 6 weeks

Secondary Outcomes (3)

  • Resilience

    From baseline to end of follow-up assessment at 10 weeks

  • Depression, anxiety, and stress

    From baseline to end of follow-up assessment at 10 weeks

  • Disturbances in self-organization

    From baseline to end of follow-up assessment at 10 weeks

Study Arms (2)

Digitalized, AI-based web app

EXPERIMENTAL

In the experimental arm, materials of the resilience-building psychoeducation are delivered through an interactive web app. Based on users' assessment responses (i.e., multiple choice and free-text questions), an integrated AI-based recommender system using a hybrid filtering approach will identify and deliver suitable resilience-building strategies.

Behavioral: Digitalized Session 1 of Mission ReST

In-person delivery

ACTIVE COMPARATOR

In the active comparator arm, the structurally and time-equivalent modules are delivered by trained facilitators.

Behavioral: In-person delivery of Mission ReST Session 1

Interventions

The interactive web app is integrated with an AI-based recommender system using a hybrid filtering approach that will identify and deliver suitable strategies based on users' assessment responses (i.e., multiple choice and free-text questions).

Digitalized, AI-based web app

Structurally and time equivalent to the digital version of Mission ReST Session 1, delivered by a trained facilitator after assessing the participant's concerns and responses.

In-person delivery

Eligibility Criteria

Age18 Years - 24 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Undergraduate at PolyU
  • Able to provide informed consent
  • Report normal to moderate levels of distress as measured by DASS-21

You may not qualify if:

  • Severe or higher levels of mental distress as measured by DASS-21
  • Self-report diagnosis of mental illness
  • Currently receiving professional mental health services

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

School of Nursing, The Hong Kong Polytechnic University

Hong Kong, Hong Kong

Location

Related Publications (11)

  • Cloitre M, Shevlin M, Brewin CR, Bisson JI, Roberts NP, Maercker A, Karatzias T, Hyland P. The International Trauma Questionnaire: development of a self-report measure of ICD-11 PTSD and complex PTSD. Acta Psychiatr Scand. 2018 Dec;138(6):536-546. doi: 10.1111/acps.12956. Epub 2018 Sep 3.

    PMID: 30178492BACKGROUND
  • Handley MA, Lyles CR, McCulloch C, Cattamanchi A. Selecting and Improving Quasi-Experimental Designs in Effectiveness and Implementation Research. Annu Rev Public Health. 2018 Apr 1;39:5-25. doi: 10.1146/annurev-publhealth-040617-014128. Epub 2018 Jan 12.

    PMID: 29328873BACKGROUND
  • Hedberg EC, Ayers S. The power of a paired t-test with a covariate. Soc Sci Res. 2015 Mar;50:277-91. doi: 10.1016/j.ssresearch.2014.12.004. Epub 2014 Dec 17.

    PMID: 25592936BACKGROUND
  • Ho GWK, Karatzias T, Cloitre M, Chan ACY, Bressington D, Chien WT, Hyland P, Shevlin M. Translation and validation of the Chinese ICD-11 International Trauma Questionnaire (ITQ) for the Assessment of Posttraumatic Stress Disorder (PTSD) and Complex PTSD (CPTSD). Eur J Psychotraumatol. 2019 May 15;10(1):1608718. doi: 10.1080/20008198.2019.1608718. eCollection 2019.

    PMID: 31143410BACKGROUND
  • Smith BW, Dalen J, Wiggins K, Tooley E, Christopher P, Bernard J. The brief resilience scale: assessing the ability to bounce back. Int J Behav Med. 2008;15(3):194-200. doi: 10.1080/10705500802222972.

    PMID: 18696313BACKGROUND
  • Henry JD, Crawford JR. The short-form version of the Depression Anxiety Stress Scales (DASS-21): construct validity and normative data in a large non-clinical sample. Br J Clin Psychol. 2005 Jun;44(Pt 2):227-39. doi: 10.1348/014466505X29657.

    PMID: 16004657BACKGROUND
  • Achilles MR, Anderson M, Li SH, Subotic-Kerry M, Parker B, O'Dea B. Adherence to e-mental health among youth: Considerations for intervention development and research design. Digit Health. 2020 May 21;6:2055207620926064. doi: 10.1177/2055207620926064. eCollection 2020 Jan-Dec.

    PMID: 32547775BACKGROUND
  • Karatzias T, Mc Glanaghy E, Cloitre M. Enhanced Skills Training in Affective and Interpersonal Regulation (ESTAIR): A New Modular Treatment for ICD-11 Complex Posttraumatic Stress Disorder (CPTSD). Brain Sci. 2023 Sep 9;13(9):1300. doi: 10.3390/brainsci13091300.

    PMID: 37759901BACKGROUND
  • Abulfaraj GG, Upsher R, Zavos HMS, Dommett EJ. The Impact of Resilience Interventions on University Students' Mental Health and Well-Being: A Systematic Review. Educ Sci. 2024;14(5)doi:10.3390/educsci14050510

    BACKGROUND
  • Ang WHD, Lau ST, Cheng LJ, et al. Effectiveness of resilience interventions for higher education students: A meta-analysis and metaregression. J Educ Psychol. 2022;114(7):1670-1694. doi:10.1037/edu0000719

    BACKGROUND
  • Masten AS, Lucke CM, Nelson KM, Stallworthy IC. Resilience in Development and Psychopathology: Multisystem Perspectives. Annu Rev Clin Psychol. 2021 May 7;17:521-549. doi: 10.1146/annurev-clinpsy-081219-120307. Epub 2021 Feb 3.

    PMID: 33534615BACKGROUND

Study Officials

  • Grace WK Ho, PhD

    The Hong Kong Polytechnic University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: A Pragmatic, Preference-Based, Open-Label, Non-Randomized Trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

July 17, 2026

First Posted

October 1, 2026

Study Start (Estimated)

November 1, 2026

Primary Completion (Estimated)

June 30, 2027

Study Completion (Estimated)

June 30, 2027

Last Updated

October 1, 2026

Record last verified: 2026-09

Locations