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CARE Study for Paramedics in Singapore

Cognitive Training And Resilience Education (CARE) for Paramedics on the Frontlines of the COVID-19 Epidemic: A Randomised Controlled Trial in Singapore

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07457801
Enrollment
63
Registered
2026-03-09
Start date
2020-09-12
Completion date
2025-06-30
Last updated
2026-03-09

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

Conditions

Anxiety Disorders and Symptoms, Burnout, Depression, Post Traumatic Stress Disorder, Psychological Distress

Brief summary

The purpose of this study is to compare the effectiveness of two different online education courses (Oxford-Online and Mind-Online) for preventing stress related conditions among paramedics who have been working during a period of COVID-19 occurrence in Singapore. The study aims to: * Compare the efficacy of a locally-adapted version of internet-delivered cognitive training for resilience (Oxford Online) to an existing educational online training (Mind Online) on depressive symptom severity * Compare the efficacy of Oxford Online to Mind Online for improving posttraumatic stress symptoms, resilience, general psychological distress, anxiety symptoms, social support, work engagement, and health-related quality of life Participants will: * Complete an online battery of baseline questionnaires * Be randomised to receive 6 modules of either Oxford Online or Mind Online, delivered once per week over a 6-week period * Complete the same online questionnaire battery immediately following the intervention, and again at the 6-month and 12-month follow up

Detailed description

Aim 1 (Primary): To compare the efficacy of a locally-adapted version of internet-delivered cognitive training for resilience (Oxford Online) to an existing educational online training (Mind Online) on depressive symptom severity in a sample of paramedics recruited during the COVID-19 pandemic in Singapore. Aim 2 (Secondary): To compare the efficacy of Oxford-Online to Mind-Online for improving posttraumatic stress symptoms, resilience, general psychological distress, anxiety symptoms, social support, work engagement, and health-related quality of life in a sample of paramedics recruited during the COVID-19 pandemic in Singapore. Aim 3 (Economic): To evaluate the incremental cost and cost-effectiveness of Oxford Online in a sample of paramedics recruited during the COVID-19 pandemic in Singapore.

Interventions

BEHAVIORALOxford-Online

The Oxford Online programme targets cognitive predictors of depression and posttraumatic stress disorder. The core information is delivered in six 20-minute modules over a 6-week period. The modules include whiteboard videos to explain concepts, audio files for practicing concrete thinking, video testimonies and footage of paramedics on-call for use in experiential exercises. A trained online wellbeing coordinator will provide individual email feedback on participants' responses and send brief automated message reminders.

BEHAVIORALMind-Online

Mind Online is a series of six modules available online where participants read information and advice about stress, depression, posttraumatic stress, sleep problems, anger, and mindfulness. A trained online wellbeing coordinator will provide individual email feedback on participants' responses and send brief automated message reminders.

Sponsors

Singapore General Hospital
Lead SponsorOTHER
Duke-NUS Graduate Medical School
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Parallel group block RCT design

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age 21 and above * English speaking * Employed or subcontracted as paramedics by SCDF who have been working during the COVID-19 pandemic * Able to provide informed consent and read study materials * Willing to enter randomised trial

Exclusion criteria

* Non-English speaking * Not working during COVID-19 outbreak (e.g. on medical or maternity leave) * Working as trainees, conscripts, medics or ambulance drivers * Unwilling or unable to complete study procedures * Unwilling to enter randomised trial

Design outcomes

Primary

MeasureTime frameDescription
Change in Depression SymptomsChange from baseline at post-intervention (6-8 weeks after baseline), 6 months and 12 months post-interventionPatient Health Questionnaire 9 (PHQ-9)

Secondary

MeasureTime frameDescription
Change in Posttraumatic Stress SymptomsChange from baseline at post-intervention (6-8 weeks after baseline), 6 months and 12 months post-interventionPosttraumatic Stress Disorder Checklist for DSM-5 (PCL-5)
Change in ResilienceChange from baseline at post-intervention (6-8 weeks after baseline), 6 months and 12 months post-interventionConnor-Davidson Resilience Scale (CD-RISC)
Change in RuminationChange from baseline at post-intervention (6-8 weeks after baseline), 6 months and 12 months post-interventionResponse to Intrusions Questionnaire (RIQ-s)
Change in Anxiety SymptomsChange from baseline at post-intervention (6-8 weeks after baseline), 6 months and 12 months post-interventionGeneralized Anxiety Disorder seven item scale (GAD-7)
Change in Psychological DistressChange from baseline at post-intervention (6-8 weeks after baseline), 6 months and 12 months post-interventionGeneral Health Questionnaire (GHQ)
Change in BurnoutChange from baseline at post-intervention (6-8 weeks after baseline), 6 months and 12 months post-interventionPhysician Work-Life Study's Single Item (PWLS)
Change in Social SupportChange from baseline at post-intervention (6-8 weeks after baseline), 6 months and 12 months post-interventionMultidimensional Scale of Perceived Social Support (MSPSS)
Change in Work EngagementChange from baseline at post-intervention (6-8 weeks after baseline), 6 months and 12 months post-interventionUtrecht Work Engagement Scale (UWES)
Change in Health-related Quality of LifeChange from baseline at post-intervention (6-8 weeks after baseline), 6 months and 12 months post-interventionEuroQol 5 Dimensions Questionnaire (EQ-5D5L)
Change in Posttraumatic GrowthChange from baseline at 6 months and 12 months post-intervention (intervention completed 6-8 weeks after baseline).Posttraumatic Growth Inventory (PTGI-SF)

Countries

Singapore

Contacts

PRINCIPAL_INVESTIGATORGayathri Devi Nadarajan

SGH

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026