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Reducing Individual Work Stress in Healthcare Professionals Through Exchange of Job Resources

E

Erasmus University Rotterdam

Status

Not yet enrolling

Conditions

Job Crafting

Study type

Observational

Funder types

Other

Identifiers

NCT06853561
ETH2425-0324
14160503.001 (Other Grant/Funding Number)

Details and patient eligibility

About

The present study focuses on prosocial job crafting as a novel strategy to reduce burnout and foster well-being among nurse professionals. Specifically, we will examine whether prosocial job crafting enhances individual and team-level well-being by increasing own and others' resources.

Full description

Below, we provide more information on the study design, study procedure, data collection, data management, and data analysis.

Study Design:

Type: Prospective, longitudinal, observational diary study. Duration: 10 workdays of daily surveys with a baseline survey at the start (Day 0).

Setting: Online survey tool (Castor), accessible via smartphones.

Study Procedure:

Day 0 - Baseline Survey: Collects demographic data and job-related information.

Days 1-10 - Daily Surveys:

Workday Verification: Confirmation of work on that day.

In addition to the outcomes listed under primary and secondary outcome measures, daily surveys will include measures of:

Prosocial Job Crafting: 12 items adapted to measure crafting behaviors to benefit other team members, using the Prosocial Job Crafting Measure (PSJCM).

Psychological Capital: 12 items measuring hope, self-efficacy, optimism, and resilience, using a shortened version of the Psychological Capital Questionnaire (PCQ).

Day 11 - Post-Study Survey: Summary of results and feedback opportunity.

Data Collection:

Survey Platform: Mobile-friendly (Castor). Questionnaire Format: Self-report measures adapted for daily context.

Data Management:

Anonymity: Participants are assigned anonymous codes for data matching. Confidentiality: Data is securely stored with access only for researchers on the project.

Statistical Analysis:

Multilevel modeling will be used to analyze the nested nature of daily data and relationships between job crafting, resource exchange, and work outcomes.

Enrollment

75 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Eligibility Criteria:

  • Employees (nurse professionals) working in a team-based work environment (hospital setting).
  • Participants must be able to complete daily surveys in the designated timeframe (end of each workday).

Exclusion Criteria:

  • Part-time workers with small contracts (less than 3 days a week) or individuals not engaged in team-based work.
  • Participants who do not complete the baseline survey or a minimum of 5 daily surveys.

Trial design

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Luisa Solms, MSc

Data sourced from clinicaltrials.gov

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