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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06169293
Other study ID # NUS-IRB-2023-641
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date December 25, 2023
Est. completion date August 31, 2024

Study information

Verified date December 2023
Source National University of Singapore
Contact Darryl Ang, PhD
Phone 66011298
Email darrylang@nus.edu.sg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date August 31, 2024
Est. primary completion date August 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - 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 Exclusion Criteria: - Students who refused to participate in the study

Study Design


Intervention

Behavioral:
I-AM-WELL
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.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
National University of Singapore

Outcome

Type Measure Description Time frame Safety issue
Primary Resilience Brief Resilience Scale Before training
Primary Resilience Brief Resilience Scale Immediately after training
Primary Depression, Anxiety and Stress Depression, Anxiety and Stress Scale - 21 Before training
Primary Depression, Anxiety and Stress Depression, Anxiety and Stress Scale - 21 Immediately after training
Primary Practice Readiness Nursing Practice Readiness Scale Before training
Primary Practice Readiness Nursing Practice Readiness Scale Immediately after training
Primary Physical Activity International Physical Activity Questionnaire Before training
Primary Physical Activity International Physical Activity Questionnaire Immediately after training
Primary Eating behaviours Self-regulation of eating behaviours scale Before training
Primary Eating behaviours Self-regulation of eating behaviours scale Immediately after training
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