ResilienceI-AM-WELLNCT06169293
Evaluation of an Interactive Mental Wellness (I-AM-WELL) Program on Final Year Nursing Students
A study testing I-AM-WELL in people with Resilience and Practice Readiness, run by National University of Singapore.
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. Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Resilience, Practice Readiness, Depression
- What is being tested?
- I-AM-WELL
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 200 participants
- Where
- No sites listed yet
- Study dates
- 25 Dec 2023to 31 Aug 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- 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
Who cannot join
- Students who refused to participate in the study
Trial locations and contacts
No sites are listed yet.
About this study
Official title: 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
- Conditions
- Resilience, Practice Readiness, Depression, Anxiety, Stress, Physical Activity
- Being tested
- I-AM-WELL
- Medical subject headings
- Depression, Anxiety Disorders, Motor Activity, Feeding Behavior
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
I-AM-WELLBehavioural
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.
| Study group | Role | What they receive |
|---|---|---|
| I-AM-WELL program | Experimental | Not described Receives: Behavioral: I-AM-WELL |
| Waitlist control | No intervention | Students will receive the intervention after data is collected from all three time points |
What is being measured
The primary outcome is the main question the study is designed to answer.
Resilience
Brief Resilience Scale
Measured: Before training
Resilience
Brief Resilience Scale
Measured: Immediately after training
Depression, Anxiety and Stress
Depression, Anxiety and Stress Scale - 21
Measured: Before training
Depression, Anxiety and Stress
Depression, Anxiety and Stress Scale - 21
Measured: Immediately after training
Practice Readiness
Nursing Practice Readiness Scale
Measured: Before training
Practice Readiness
Nursing Practice Readiness Scale
Measured: Immediately after training
Physical Activity
International Physical Activity Questionnaire
Measured: Before training
Physical Activity
International Physical Activity Questionnaire
Measured: Immediately after training
Eating behaviours
Self-regulation of eating behaviours scale
Measured: Before training
Eating behaviours
Self-regulation of eating behaviours scale
Measured: Immediately after training
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Dec 2023
- Study start25 Dec 2023 (estimated)
- Primary completion31 Aug 2024 (estimated)
- Study completion31 Aug 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for ResilienceStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Care provider, Outcomes assessor
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- National University of Singapore
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Darryl Ang, PhD, Principal investigator, National University of Singapore
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06169293
- Sponsor's protocol ID
- NUS-IRB-2023-641
- Acronym
- I-AM-WELL
- Status last verified
- Dec 2023
- First submitted
- 1 Dec 2023
- Last updated
- 13 Dec 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 13 Dec 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of an Interactive Mental Wellness (I-AM-WELL) Program on Final Year Nursing Students: A Mixed Methods Evaluation
- ClinicalTrials.gov ID
- NCT06169293
- Acronym / sponsor ID
- I-AM-WELL / NUS-IRB-2023-641
- Conditions
- Resilience, Practice Readiness, Depression, Anxiety, Stress, Physical Activity
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- National University of SingaporeUniversity, hospital or other
- Study start
- 25 Dec 2023 (estimated)
- Primary completion
- 31 Aug 2024 (estimated)
- Study completion
- 31 Aug 2024 (estimated)
- First posted
- 13 Dec 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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 design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (care provider, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| 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 |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- 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
Key exclusion criteria (1 listed)
- Students who refused to participate in the study
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| I-AM-WELLThe 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. | Behavioural | I-AM-WELL program |
Primary outcome
Resilience
Time frame: Before training
Brief Resilience Scale
Resilience
Time frame: Immediately after training
Brief Resilience Scale
Depression, Anxiety and Stress
Time frame: Before training
Depression, Anxiety and Stress Scale - 21
Depression, Anxiety and Stress
Time frame: Immediately after training
Depression, Anxiety and Stress Scale - 21
Practice Readiness
Time frame: Before training
Nursing Practice Readiness Scale
Practice Readiness
Time frame: Immediately after training
Nursing Practice Readiness Scale
Physical Activity
Time frame: Before training
International Physical Activity Questionnaire
Physical Activity
Time frame: Immediately after training
International Physical Activity Questionnaire
Eating behaviours
Time frame: Before training
Self-regulation of eating behaviours scale
Eating behaviours
Time frame: Immediately after training
Self-regulation of eating behaviours scale
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Dec 2023.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Darryl Ang, PhD principal investigator
National University of Singapore
Questions about this trial
What is this clinical trial studying?
A study testing I-AM-WELL in people with Resilience and Practice Readiness, run by National University of Singapore.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 13 Dec 2023. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Darryl Ang, PhD (66011298, darrylang@nus.edu.sg), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Resilience (time frame: Before training). The study lists 10 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Dec 2023.