- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07402187
"Productivity Training and Job Stress Among Nurses"
The Effect of Productivity Training on Perceived Job Stress and Productivity Attitudes Among Nurses: A Randomized Controlled Experimental Study
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Neslihan Erim
- Phone Number: +90 537 344 2913
- Email: neslihanerim24@istanbularel.edu.tr
Study Contact Backup
- Name: Seyhan Çerçi, Dr. Öğretim Üyesi
- Phone Number: +90 506 467 98 35
- Email: mseyhancerci@gmail.com
Study Locations
-
-
-
Istanbul, Turkey (Türkiye)
- Recruiting
- Istanbul University Istanbul Faculty of Medicine
-
Contact:
- Neslihan E Master's Degree, Student
- Phone Number: 05373442913
- Email: neslihankurtt.1994@gmail.com
-
-
Istanbul
-
Istanbul, Istanbul, Turkey (Türkiye), 34000
- Not yet recruiting
- Istanbul Arel University
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
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:
- Not being a nurse
- Being over 65 years old
- Not volunteering to participate in the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
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.
|
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. |
|
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.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Nurses' Attitude Scale Regarding Productivity
Time Frame: Time Frame: At baseline (before the training), immediately after the 3-week productivity training program, and 3 months after the training.
|
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: At baseline (before the training), immediately after the 3-week productivity training program, and 3 months after the training.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Work Stress Scale (PWSS)
Time Frame: Time Frame: At baseline (before the training), immediately after the 3-week productivity training program, and 3 months
|
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: At baseline (before the training), immediately after the 3-week productivity training program, and 3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Seyhan Çerçi, Dr. Öğretim Üyesi, Bağlantısız
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025/16
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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