Effect of an Empowerment-Based Psychoeducation Program on Burnout and Psychological Outcomes in Nurse Managers
EMPOWER-NM
The Effect of an Empowerment-Based Psychoeducation Program on Burnout, Self-Leadership, Psychological Empowerment, and Psychological Resilience in Nurse Managers: A Randomized Controlled Trial
1 other identifier
interventional
60
1 country
1
Brief Summary
This randomized controlled trial aims to evaluate the effectiveness of an empowerment-based psychoeducation program on burnout, self-leadership, mindfulness, and psychological resilience among nurse managers. The study population consists of nurse managers working in healthcare settings. The primary objective of this study is to determine whether the psychoeducation program reduces burnout levels and improves self-leadership, mindfulness, and psychological resilience among nurse managers. The main research questions are as follows: Does the empowerment-based psychoeducation program reduce burnout levels in nurse managers? Does the program improve self-leadership levels in nurse managers? Does the program increase mindfulness levels in nurse managers? Does the program enhance psychological resilience in nurse managers? In this randomized controlled design, participants will be assigned to either an intervention group or a control group. The intervention group will receive a structured empowerment-based psychoeducation program lasting five weeks, while the control group will not receive any intervention. Participants will undergo the following procedures: Completion of baseline (pre-test) assessments (T1) Participation in the psychoeducation program for the intervention group (5 weeks) No intervention for the control group Completion of post-intervention assessments (T2) Completion of follow-up assessments three months after the intervention (T3) The findings of this study are expected to contribute to the development of evidence-based interventions aimed at strengthening managerial competencies and psychological well-being among nurse managers.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 19, 2026
CompletedFirst Posted
Study publicly available on registry
April 29, 2026
CompletedStudy Start
First participant enrolled
June 5, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
July 3, 2026
Study Completion
Last participant's last visit for all outcomes
October 5, 2026
April 29, 2026
April 1, 2026
28 days
April 19, 2026
April 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in burnout levels measured using the Maslach Burnout Inventory.
The Emotional Exhaustion subscale ranges from 0 to 36, the Depersonalization subscale ranges from 0 to 20, and the Personal Accomplishment subscale ranges from 0 to 32. Higher scores on Emotional Exhaustion and Depersonalization indicate higher levels of burnout, whereas higher scores on Personal Accomplishment indicate lower levels of burnout.
Time Frame: Baseline (T1), 5 weeks after intervention (T2), and 3-month follow-up (T3).
Secondary Outcomes (3)
Change in self-leadership levels measured using the Self-Leadership Scale.
Time Frame: Baseline (T1), 5 weeks after intervention (T2), and 3-month follow-up (T3).
Change in psychological empowerment levels measured using the Psychological Empowerment Scale.
Time Frame: Baseline (T1), 5 weeks after intervention (T2), and 3-month follow-up (T3).
Change in resilience levels measured using the Brief Resilience Scale
Baseline (T1), 5 weeks after intervention (T2), and 3 months after intervention (T3)
Study Arms (2)
Empowerment-Based Psychoeducation Group
EXPERIMENTALParticipants in this group will receive a structured empowerment-based psychoeducation program consisting of 5 sessions over 5 weeks. The program aims to improve self-leadership, psychological empowerment, mindfulness, and resilience, and to reduce burnout levels among nurse managers.
Control Group
NO INTERVENTIONParticipants in this group will not receive any intervention during the study period but will complete the same assessment schedule as the intervention group.
Interventions
A structured psychoeducation program designed to enhance self-leadership, psychological empowerment, mindfulness, and resilience, and to reduce burnout among nurse managers through interactive sessions, group discussions, and practical exercises over a 5-week period.
Eligibility Criteria
You may qualify if:
- Nurse managers currently working in healthcare institutions
- Aged 18 years or older
- Willing to participate in the study
- Able to attend all psychoeducation sessions
- Provide informed consent
You may not qualify if:
- Participation in a similar psychoeducation or intervention program within the last 6 months
- Inability to attend scheduled sessions regularly
- Refusal to provide informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Suleyman Demirel Universitylead
- Kırıkkale Universitycollaborator
Study Sites (1)
Suleyman Demirel University
Isparta, 32100, Turkey (Türkiye)
Related Links
- An on-the-job mindfulness-based intervention for pediatric ICU nurses: Study describing a mindfulness-based intervention and its effects on nurses' well-being.
- Relevant study examining burnout and psychological outcomes among healthcare professionals.
- Study evaluating interventions aimed at improving psychological well-being and resilience.
- Research examining leadership and empowerment in healthcare settings.
- Study investigating psychological empowerment and its effects on professional outcomes.
- Research focusing on resilience and psychological adaptation in healthcare professionals.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Tangul Aytur Ozen, Phd.
Suleyman Demirel University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- This study is open-label, and no masking is applied.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
April 19, 2026
First Posted
April 29, 2026
Study Start (Estimated)
June 5, 2026
Primary Completion (Estimated)
July 3, 2026
Study Completion (Estimated)
October 5, 2026
Last Updated
April 29, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
Individual participant data (IPD) will not be shared due to ethical restrictions and the need to protect participant confidentiality. Data will be reported in aggregate form only.