NCT07556302

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

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
4mo left

Started Jun 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Completed
10 days until next milestone

First Posted

Study publicly available on registry

April 29, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

June 5, 2026

Expected
28 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 3, 2026

3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 5, 2026

Last Updated

April 29, 2026

Status Verified

April 1, 2026

Enrollment Period

28 days

First QC Date

April 19, 2026

Last Update Submit

April 24, 2026

Conditions

Keywords

nurse led interventionsPsychological Empowerment programSelf-leadershipPsychological ResilienceBurnout

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

EXPERIMENTAL

Participants 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.

Behavioral: Empowerment-Based Psychoeducation Program

Control Group

NO INTERVENTION

Participants 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.

Empowerment-Based Psychoeducation Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Suleyman Demirel University

Isparta, 32100, Turkey (Türkiye)

Location

Related Links

MeSH Terms

Conditions

Burnout, Psychological

Condition Hierarchy (Ancestors)

Stress, PsychologicalBehavioral SymptomsBehavior

Study Officials

  • Tangul Aytur Ozen, Phd.

    Suleyman Demirel University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Tangul Aytur Ozen, Phd.

CONTACT

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
Model Details: Participants will be randomly assigned to either an intervention group receiving an empowerment-based psychoeducation program or a control group receiving no intervention. The intervention will last five weeks, with assessments conducted at baseline (T1), post-intervention (T2), and three-month follow-up (T3).
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.

Locations