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Occupational DisidentificationNCT07682493

Undergraduate Nursing Intern Cohort Study

An observational study of Occupational Disidentification, run by Nanjing Medical University at 1 site in China.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This prospective observational cohort study aims to examine changes in occupational disidentification among undergraduate nursing interns during clinical internship and to identify factors associated with high-risk trajectories. Read more about this study

Who is it for?
Ages 18 to 25 yearsHealthy volunteers can take part
Conditions the study is for
Occupational Disidentification
How many people
500 participants
Where
1 siteChina
Study dates
Jun 2026to Jun 2027
Phase
Observational
Are there results?
Not yet: the study is under way

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 25 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: The study population will consist of full-time undergraduate nursing students from multiple participating universities in China, including students who are about to enter or are in the early stage of clinical internship. Eligible students will be recruited using a non-probability convenience sampling method and followed prospectively through online questionnaires during the internship period.

Who may be able to join

  • Full-time undergraduate students majoring in nursing.
  • Students who are about to enter clinical internship or are in the early stage of clinical internship.
  • Students who are able to use the WeChat mini-program to complete questionnaires.
  • Students with normal reading comprehension ability.
  • Students who voluntarily agree to participate in the study and provide informed consent.

Who cannot join

  • Students who are unable to complete the internship during the study period due to suspension of schooling, withdrawal from school, military service, long-term sick leave, or other reasons.
  • Students who have participated in similar interventional studies that may affect the assessment of the primary outcome.
  • Students with severe physical or mental illness, or other conditions that make them unable to complete the questionnaires independently.
  • Questionnaires with an obviously too short completion time, below the minimum reasonable response time set by the research team.
  • Questionnaires with patterned responses or obvious logical inconsistencies.
  • Questionnaires with missing key variables that cannot be used for the main statistical analysis.
  • Repeated submissions at the same time point where the valid version cannot be confirmed.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

China1 site, 1 recruiting
  • Nanjing Medical University

    Nanjing, Jiangsu, 211166

    Jun Yao, PhD, 86-13915965527, yaojun@njmu.edu.cn

    Recruiting

Other trials in China

About this study

Official title: Risk Trajectories and Prediction Model of Occupational Disidentification Among Undergraduate Nursing Interns: A Prospective Cohort Study

This prospective observational cohort study aims to examine changes in occupational disidentification among undergraduate nursing interns during clinical internship and to identify factors associated with high-risk trajectories. Undergraduate nursing students will be followed using online questionnaires from the end of the first internship week and approximately every three months until the end of internship. The study will assess occupational disidentification, personal psychological resources, clinical learning environment, occupational stigma, negative clinical experiences, transition shock, emotional exhaustion, occupational fatigue, sleep, and musculoskeletal symptoms.

Keywords
Undergraduate Nursing Interns, Nursing Students, Clinical Internship, Occupational Disidentification, Prospective Cohort Study, Professional Identity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07682493
Study groupRoleWhat they receive
Undergraduate Nursing InternsUndergraduate nursing students who are about to enter or are in the early stage of clinical internship will be followed prospectively using online questionnaires during the internship period.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Occupational Disidentification

    Occupational disidentification refers to the tendency of undergraduate nursing interns to psychologically distance themselves from the nursing profession or separate the nursing professional identity from their self-concept. It will be assessed using an occupational disidentification scale. Higher scores indicate a higher level of occupational disidentification.

    Measured: From the end of the first internship week to the end of internship, up to 12 months

Secondary outcomes (2)
  1. Change in Transition Shock

    Transition shock refers to the instability, stress, and maladaptation experienced by undergraduate nursing interns during the transition from school-based learning to clinical practice. It will be assessed using a transition shock scale. Higher scores indicate a higher level of transition shock.

    Measured: End of the first internship week and approximately every three months until the end of internship, up to 12 months

  2. Change in Emotional Exhaustion

    Emotional exhaustion refers to the depletion of emotional and psychological resources experienced by undergraduate nursing interns during clinical internship. It will be assessed using an emotional exhaustion scale. Higher scores indicate a higher level of emotional exhaustion.

    Measured: End of the first internship week and approximately every three months until the end of internship, up to 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Jul 2026
  2. Study startJun 2026 (estimated)
  3. Primary completionJun 2027 (estimated)
  4. Study completionJun 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07682493
Sponsor's protocol ID
NJMU-IRB-2026-079
Status last verified
Jun 2026
First submitted
28 Jun 2026
Last updated
6 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared because the study involves sensitive questionnaire data from undergraduate nursing interns and data sharing is restricted by ethics approval and participant consent.

Questions about this trial

What is this clinical trial studying?

An observational study of Occupational Disidentification, run by Nanjing Medical University at 1 site in China.

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 5 inclusion and 7 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: looking for participants now, as of the sponsor's last update on 6 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

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?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Jun Yao, PhD (86-13915965527, yaojun@njmu.edu.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Occupational Disidentification (time frame: From the end of the first internship week to the end of internship, up to 12 months). 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 6 Jul 2026.

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