- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06169293
Evaluation of an Interactive Mental Wellness (I-AM-WELL) Program on Final Year Nursing Students (I-AM-WELL)
Evaluation of an Interactive Mental Wellness (I-AM-WELL) Program on Final Year Nursing Students: A Mixed Methods Evaluation
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
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Darryl Ang, PhD
- Phone Number: 66011298
- Email: darrylang@nus.edu.sg
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
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 Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: I-AM-WELL program
|
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. |
No Intervention: Waitlist control
Students will receive the intervention after data is collected from all three time points
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Resilience
Time Frame: Before training
|
Brief Resilience Scale
|
Before training
|
Resilience
Time Frame: Immediately after training
|
Brief Resilience Scale
|
Immediately after training
|
Practice Readiness
Time Frame: Before training
|
Nursing Practice Readiness Scale
|
Before training
|
Practice Readiness
Time Frame: Immediately after training
|
Nursing Practice Readiness Scale
|
Immediately after training
|
Depression, Anxiety and Stress
Time Frame: Before training
|
Depression, Anxiety and Stress Scale - 21
|
Before training
|
Depression, Anxiety and Stress
Time Frame: Immediately after training
|
Depression, Anxiety and Stress Scale - 21
|
Immediately after training
|
Physical Activity
Time Frame: Before training
|
International Physical Activity Questionnaire
|
Before training
|
Physical Activity
Time Frame: Immediately after training
|
International Physical Activity Questionnaire
|
Immediately after training
|
Eating behaviours
Time Frame: Before training
|
Self-regulation of eating behaviours scale
|
Before training
|
Eating behaviours
Time Frame: Immediately after training
|
Self-regulation of eating behaviours scale
|
Immediately after training
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Darryl Ang, PhD, National University of Singapore
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NUS-IRB-2023-641
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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