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Expressive Writing on Stress-Related and Work-Related Outcomes Among Chinese Nursing Interns

C

Changzhi Medical College

Status

Completed

Conditions

Stress, Psychological

Treatments

Other: Expressive writing
Other: Neutral writing

Study type

Interventional

Funder types

Other

Identifiers

NCT06238141
RT2023047

Details and patient eligibility

About

The goal of this interventional study is to assess the effects of an intervention on stress-related and work-related outcomes among Chinese nursing interns. The main questions it aims to answer are:

  • Does expressive writing reduce clinical practice stress and improve coping strategies in nursing interns?
  • Does expressive writing increase work engagement and perceived professional benefit among nursing interns?

Participants in the intervention group and control group will perform expressive writing and neutral writing, respectively, based on different given instructions. In both groups, writing will last for 10-15 minutes each time, twice a week, for nine weeks.

Researchers will compare the outcomes of the two groups to see if there are differences between clinical practice stress, coping strategies, work engagement, and perceived professional benefit.

Enrollment

52 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Undergraduate nursing interns in their first clinical internship (had no prior clinical practice experience)
  • Be willing to fill in questionnaires and write according to the assigned writing prompts
  • Never participated in writing therapy or stress management intervention programs

Exclusion criteria

  • Refusal to participate
  • Severe current psychological conditions
  • Undergoing any form of psychotherapy
  • With a habit of keeping diaries

Withdrawal criteria:

  • Termination of internship for whatever reason
  • Not submit writing materials twice

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

52 participants in 2 patient groups

intervention group
Experimental group
Treatment:
Other: Expressive writing
control group
Sham Comparator group
Treatment:
Other: Neutral writing

Trial documents
2

Trial contacts and locations

1

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Central trial contact

XUAN JI

Data sourced from clinicaltrials.gov

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