ClinicalTrials.gg
RecruitingNCT07682493Updated Jul 6, 2026

Undergraduate Nursing Intern Cohort Study

An observational study in Occupational Disidentification, sponsored by Nanjing Medical University. Recruiting at 1 site in China. Open to participants aged 18 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-06.

Sponsored by Nanjing Medical University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
500
Ages
18 Years to 25 Years
Sex
All
01

Study 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. 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.

02

Conditions studied

  • Occupational Disidentification

Keywords

  • Undergraduate Nursing Interns
  • Nursing Students
  • Clinical Internship
  • Occupational Disidentification
  • Prospective Cohort Study
  • Professional Identity
03

In context

Lead sponsor

Nanjing Medical University is the lead sponsor of 171 studies on the registry; 52 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

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.

Eligibility criteria

Inclusion Criteria:

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

Exclusion Criteria:

  1. 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.
  2. Students who have participated in similar interventional studies that may affect the assessment of the primary outcome.
  3. Students with severe physical or mental illness, or other conditions that make them unable to complete the questionnaires independently.

Exclusion From Analysis Criteria:

  1. Questionnaires with an obviously too short completion time, below the minimum reasonable response time set by the research team.
  2. Questionnaires with patterned responses or obvious logical inconsistencies.
  3. Questionnaires with missing key variables that cannot be used for the main statistical analysis.
  4. Repeated submissions at the same time point where the valid version cannot be confirmed.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
500 participants (estimated)
Patient registry
No

Groups and cohorts

  • Undergraduate Nursing Interns

    Undergraduate 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.

06

What researchers measure

Primary outcomes

  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.

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

Secondary outcomes

  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.

    Time frame: 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.

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

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: 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.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07682493
Responsible party
JUN YAO (Professor, Nanjing Medical University) — Principal investigator
First posted
Jul 6, 2026
Start date
Jun 2026 (estimated)
Primary completion
Jun 2027 (estimated)
Completion
Jun 2027 (estimated)
Last update
Jul 6, 2026

Study contacts

Jun Yao, PhD
Contact
yaojun@njmu.edu.cn
86-13915965527
Jun Yao, PhD
principal investigator · Nanjing Medical University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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