ResilienceNCT06128889
Evaluation of a Supporting Transition and Resilience to Clinical Nursing Education (STRONG) Study
A study testing Supporting Transition and Resilience to Clinical Nursing Education (STRONG) Program in people with Resilience and Practice Readiness, run by National University of Singapore.
Trial summary
This study aims to address the following research questions: 1. Evaluate the effectiveness of a Supporting Transition and Resilience to Clinical Nursing Education (STRONG) program on first year nursing students' anxiety, depression, stress, resilience, practice readiness, physical activity and eating behaviours. 2. 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?
- Supporting Transition and Resilience to Clinical Nursing Education (STRONG) Program
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 300 participants
- Where
- No sites listed yet
- Study dates
- 1 Dec 2023to 1 Jun 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
- First year nursing students enrolled in the NUR1107B Nursing Practice Experience and NUR1202C Clinical Experience I module
- 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 this study
Trial locations and contacts
No sites are listed yet.
About this study
Official title: Evaluation of a Supporting Transition and Resilience to Clinical Nursing Education (STRONG) Study - A Mixed Methods Evaluation
This study aims to address the following research questions:
- Evaluate the effectiveness of a Supporting Transition and Resilience to Clinical Nursing Education (STRONG) program on first year nursing students' anxiety, depression, stress, resilience, practice readiness, physical activity and eating behaviours.
- Explore first year nursing students' experiences and perception of the STRONG program.
Participants will be invited to participate in an asynchronous online STRONG program
- Conditions
- Resilience, Practice Readiness, Depression, Anxiety, Stress, Physical Activity
- Being tested
- Supporting Transition and Resilience to Clinical Nursing Education (STRONG) Program
- Medical subject headings
- Depression, Anxiety Disorders, Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Supporting Transition and Resilience to Clinical Nursing Education (STRONG) ProgramBehavioural
The STRONG 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 |
|---|---|---|
| STRONG program | Experimental | Not described Receives: Behavioral: Supporting Transition and Resilience to Clinical Nursing Education (STRONG) Program |
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
Resilience
Brief Resilience Scale
Measured: 1 month 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
Depression, Anxiety, and Stress
Depression, Anxiety and Stress Scale - 21
Measured: 1 month after training
Practice Readiness
Nursing Practice Readiness Scale
Measured: Before training
Practice Readiness
Nursing Practice Readiness Scale
Measured: Immediately after training
Practice Readiness
Nursing Practice Readiness Scale
Measured: 1 month after training
Physical activity
International Physical Activity Questionnaire
Measured: Before training
Physical activity
International Physical Activity Questionnaire
Measured: Immediately after training
Physical activity
International Physical Activity Questionnaire
Measured: 1 month 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
Eating behaviours
Self-regulation of Eating Behaviours Scale
Measured: 1 month 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 Nov 2023
- Study start1 Dec 2023 (estimated)
- Primary completion1 Apr 2024 (estimated)
- Study completion1 Jun 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.
- More trials run by National University of SingaporeThe sponsor's other registered studies.
- 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
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 300 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
- NCT06128889
- Sponsor's protocol ID
- NUS-IRB-2023-737
- Status last verified
- Dec 2023
- First submitted
- 2 Nov 2023
- Last updated
- 8 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 8 Dec 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of a Supporting Transition and Resilience to Clinical Nursing Education (STRONG) Study - A Mixed Methods Evaluation
- ClinicalTrials.gov ID
- NCT06128889
- Acronym / sponsor ID
- NUS-IRB-2023-737
- Conditions
- Resilience, Practice Readiness, Depression, Anxiety, Stress, Physical Activity
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 300 participants (estimated)
- Lead sponsor
- National University of SingaporeUniversity, hospital or other
- Study start
- 1 Dec 2023 (estimated)
- Primary completion
- 1 Apr 2024 (estimated)
- Study completion
- 1 Jun 2024 (estimated)
- First posted
- 13 Nov 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 a Supporting Transition and Resilience to Clinical Nursing Education (STRONG) program on first year nursing students' anxiety, depression, stress, resilience, practice readiness, physical activity and eating behaviours.
- Explore first year nursing students' experiences and perception of the STRONG program.
Participants will be invited to participate in an asynchronous online STRONG program
Study design
- Primary purpose
- Prevention
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| STRONG program | Experimental | Behavioral: Supporting Transition and Resilience to Clinical Nursing Education (STRONG) Program |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- First year nursing students enrolled in the NUR1107B Nursing Practice Experience and NUR1202C Clinical Experience I module
- 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 this 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 |
|---|---|---|
| Supporting Transition and Resilience to Clinical Nursing Education (STRONG) ProgramThe STRONG 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 | STRONG program |
Primary outcome
Resilience
Time frame: Before training
Brief Resilience Scale
Resilience
Time frame: Immediately after training
Brief Resilience Scale
Resilience
Time frame: 1 month 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
Depression, Anxiety, and Stress
Time frame: 1 month 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
Practice Readiness
Time frame: 1 month 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
Physical activity
Time frame: 1 month 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
Eating behaviours
Time frame: 1 month 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 8 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 Supporting Transition and Resilience to Clinical Nursing Education (STRONG) Program 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 8 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 15 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 8 Dec 2023.