NCT06169293

Brief Summary

This study aims to address the following research questions: Evaluate the effectiveness of an Interactive Mental Wellness (I-AM-WELL) program on final year nursing students' anxiety, depression, stress, resilience, practice readiness, physical activity and eating behaviours. Explore final year nursing students' experiences and perception of the I-AM-WELL program. Participants will be invited to participate in an asynchronous online I-AM-WELL program

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Dec 2023

Shorter than P25 for not_applicable

Status
unknown

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 1, 2023

Completed
12 days until next milestone

First Posted

Study publicly available on registry

December 13, 2023

Completed
12 days until next milestone

Study Start

First participant enrolled

December 25, 2023

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2024

Completed
Last Updated

December 13, 2023

Status Verified

December 1, 2023

Enrollment Period

8 months

First QC Date

December 1, 2023

Last Update Submit

December 5, 2023

Conditions

Outcome Measures

Primary Outcomes (10)

  • Resilience

    Brief Resilience Scale

    Before training

  • Resilience

    Brief Resilience Scale

    Immediately after training

  • Depression, Anxiety and Stress

    Depression, Anxiety and Stress Scale - 21

    Before training

  • Depression, Anxiety and Stress

    Depression, Anxiety and Stress Scale - 21

    Immediately after training

  • Practice Readiness

    Nursing Practice Readiness Scale

    Before training

  • Practice Readiness

    Nursing Practice Readiness Scale

    Immediately after training

  • Physical Activity

    International Physical Activity Questionnaire

    Before training

  • Physical Activity

    International Physical Activity Questionnaire

    Immediately after training

  • Eating behaviours

    Self-regulation of eating behaviours scale

    Before training

  • Eating behaviours

    Self-regulation of eating behaviours scale

    Immediately after training

Study Arms (2)

I-AM-WELL program

EXPERIMENTAL
Behavioral: I-AM-WELL

Waitlist control

NO INTERVENTION

Students will receive the intervention after data is collected from all three time points

Interventions

I-AM-WELLBEHAVIORAL

The I-AM-WELL program adopts an asynchronous online learning approach and will be delivered over one week by a trained counsellor, and a nurse researcher. Students will attend an online self-paced program. The program will comprise of topics such as: (1) Resilience and protective factors, (2) introduction to clinical nursing education, (3) experiences of clinical attachments, and (4) stress, physical wellbeing and diet materials. Students will have access to online materials (e.g., short videos), have opportunities to discuss (e.g., forum) and infographics. Overall, the program will be delivered over in one week lasting six hours.

I-AM-WELL program

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Final year nursing students enrolled in the undergraduate nursing program
  • Above the ages of 18 years
  • Able to comprehend the English language
  • Have a device that can connect to the Internet

You may not qualify if:

  • Students who refused to participate in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

DepressionAnxiety DisordersMotor ActivityFeeding Behavior

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorMental DisordersBehavior, Animal

Study Officials

  • Darryl Ang, PhD

    National University of Singapore

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Darryl Ang, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
CARE PROVIDER, OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 1, 2023

First Posted

December 13, 2023

Study Start

December 25, 2023

Primary Completion

August 31, 2024

Study Completion

August 31, 2024

Last Updated

December 13, 2023

Record last verified: 2023-12