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RecruitingNCT07402187Updated Feb 11, 2026

"Productivity Training and Job Stress Among Nurses"

An interventional study of Productivity Training Program for Nurses in Occupational Stress and Productivity, sponsored by Istanbul Arel University. Recruiting at 2 sites in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-11.

Sponsored by Istanbul Arel University · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Primary completion was expected by Apr 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started Nov 2025; still recruiting 11 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
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Study summary

This study aims to examine the effect of productivity training on nurses' perceived job stress and attitudes toward productivity. It was designed as a randomized controlled experimental study with a pre-test, post-test, and follow-up design. The experimental group will receive a three-week structured productivity training program, while the control group will not receive any intervention during the same period. Data will be collected using the Personal Information Form, the Nurses' Attitudes Toward Productivity Scale, and the Perceived Job Stress Scale. It is hypothesized that nurses who participate in the productivity training will report lower perceived job stress and higher productivity attitudes compared to those in the control group.

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Conditions studied

  • Occupational Stress
  • Productivity

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Keywords

  • Nursing
  • job stress
  • Productivity
  • Randomized Controlled Trial
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In context

Occupational Stress

236 studies on the registry are indexed under Occupational Stress; 63 are open to participants now.

This study's planned enrollment of 70 is below the median of 84 across 168 interventional studies indexed under Occupational Stress.

Browse Occupational Stress studies →

Lead sponsor

Istanbul Arel University is the lead sponsor of 44 studies on the registry; 14 are open to participants now.

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

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Being a nurse
  • Being over 18 years old
  • Working in the institution for at least 3 months
  • Volunteering to participate in the study

Exclusion criteria

Exclusion Criteria:

  • Not being a nurse
  • Being over 65 years old
  • Not volunteering to participate in the study
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Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
70 participants (estimated)

Study arms

  • Experimental
    Productivity Training Program

    Participants in the experimental group will receive a structured productivity training program lasting three weeks and totaling 20 hours. The training covers topics such as the concept of productivity in nursing, time and stress management, process improvement, teamwork, leadership, the use of digital tools, and coping with job stress. Each week, various teaching methods including lectures, case analyses, simulations, practical exercises, group work, and brainstorming sessions will be used. The program aims to enhance participants' cognitive, affective, and practical competencies related to productivity and stress management in nursing practice.

    Behavioral: Productivity Training Program for Nurses

  • No intervention
    No Training Control Group

    Participants in the control group will not receive any training during the study period. They will complete the same pre-test, post-test, and follow-up assessments as the experimental group. After the completion of data collection, the productivity training materials will be made available to control group participants to ensure ethical fairness.

Interventions

  • BehavioralProductivity Training Program for Nurses

    The intervention consists of a structured productivity training program designed for nurses, delivered over three weeks (total 20 hours). The program includes interactive theoretical and practical sessions covering topics such as: The concept and scope of productivity in nursing, Time and stress management, Process improvement and teamwork, Leadership and performance support mechanisms, Coping with job stress and building psychological resilience, Use of digital tools and technology to enhance efficiency. Various teaching methods are employed, including lectures, simulations, case analyses, group discussions, applied exercises, and brainstorming. The program aims to improve nurses' cognitive, affective, and practical skills related to productivity, while reducing perceived job stress.

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What researchers measure

Primary outcomes

  1. Nurses' Attitude Scale Regarding Productivity

    Nurses' attitudes toward productivity will be assessed using the Nurses' Attitudes Toward Productivity Scale (NAPTS), developed and validated by Göktepe and Baykal (2012). The scale consists of 39 items and five subscales: professional commitment, working conditions, job demands, teamwork, and rewarding. Items are rated on a 5-point Likert scale ranging from 1 (strongly disagree) to 5 (strongly agree). Total and subscale scores are converted to a 0-100 scale, with higher scores indicating a more positive attitude toward productivity, and lower scores indicating a negative attitude toward productivity. Minimum score: 0 Maximum score: 100

    Time frame: Time Frame: At baseline (before the training), immediately after the 3-week productivity training program, and 3 months after the training.

Secondary outcomes

  1. Perceived Work Stress Scale (PWSS)

    Perceived job stress levels of the participants will be assessed using the Perceived Job Stress Scale (PJSS), originally developed by Cohen and Williamson (1988) and adapted into Turkish by Baltaş (1998). The scale consists of 15 items rated on a 5-point Likert scale. The total score is calculated by taking the mean score of the 15 items. Based on the mean score, stress levels are categorized into six groups: A (3.5-4.0) B (1.0-1.3) C (1.4-1.9) D (2.0-2.5) E (2.6-3.1) F (3.2-3.4) Higher scores indicate higher perceived job stress. Stress levels classified as A, B, E, and F are considered stress levels that may negatively affect work efficiency and threaten health, whereas C represents stress levels suitable for individuals who prefer low challenge, and D represents the optimal stress level for health and productivity. Minimum score: 1.0 Maximum score: 4.0

    Time frame: Time Frame: At baseline (before the training), immediately after the 3-week productivity training program, and 3 months

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Study locations

1 of 2 sites recruiting
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References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No — Individual participant data (IPD) will not be shared because the dataset contains sensitive personal and occupational information about nurses. Data will be analyzed and reported in aggregate form only. Access to anonymized data may be considered upon reasonable request and ethics committee approval.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07402187
Lead sponsor
Istanbul Arel University
Responsible party
Sponsor
First posted
Feb 11, 2026
Start date
Nov 18, 2025
Primary completion
Apr 18, 2026 (estimated)
Completion
Jul 18, 2026 (estimated)
Last update
Feb 11, 2026

Study contacts

Neslihan Erim
Contact
neslihanerim24@istanbularel.edu.tr
+90 537 344 2913
Seyhan Çerçi, Dr. Öğretim Üyesi
Contact
mseyhancerci@gmail.com
+90 506 467 98 35
Seyhan Çerçi, Dr. Öğretim Üyesi
principal investigator · bağlantısız

Oversight

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

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