Balint Approach Group Intervention
Balint Group
The Effect of Balint Approach Group Intervention on Burnout and Communication Skills in Nurses
1 other identifier
interventional
30
1 country
1
Brief Summary
This randomized controlled trial evaluated the effect of a Balint-based group intervention on burnout and communication skills among nurses. Burnout is a common outcome of prolonged exposure to workplace stressors and can weaken nurses' empathy, emotional regulation, and therapeutic communication abilities. Balint groups are reflective, structured sessions that focus on understanding the emotional and relational aspects of challenging patient-nurse interactions. These groups provide a safe environment for nurses to explore their thoughts and feelings, enhance self-awareness, and improve interpersonal effectiveness. The study used a two-arm parallel-group randomized controlled design with pre-test and post-test measurements and follow-up assessments at one and three months. A total of 50 nurses were screened, and 30 who met the inclusion criteria were enrolled and randomly assigned to the intervention (n = 15) or control (n = 15) group. Inclusion criteria included at least one year of experience in the same clinical setting and the provision of informed consent. Nurses with communication impairments that could interfere with participation were excluded. The intervention consisted of six weekly online Balint-based group sessions lasting 45-50 minutes. Sessions followed the structure recommended by the International Balint Federation, including case presentation, exploration, group discussion, feedback, and closing phases. The first session included additional time to review study procedures and establish group rules and confidentiality. The control group continued routine work without receiving any additional psychosocial support. The primary outcome was burnout, measured with the Maslach Burnout Inventory. The secondary outcome was communication skills, assessed with the Communication Skills Scale for Health Professionals. Both outcomes were measured at baseline, immediately after the intervention, and at one- and three-month follow-ups. Data were collected electronically, and all participants provided informed consent online. Ethical approval was obtained from the relevant institutional ethics committee. This study contributes to the growing evidence supporting the use of Balint-based reflective group interventions to enhance nurses' psychosocial well-being and professional communication competencies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Dec 2024
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
Study Start
First participant enrolled
December 20, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 5, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 5, 2025
CompletedFirst Submitted
Initial submission to the registry
November 28, 2025
CompletedFirst Posted
Study publicly available on registry
December 11, 2025
CompletedDecember 11, 2025
November 1, 2025
4 months
November 28, 2025
November 28, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Burnout (Maslach Burnout Inventory Total Score)
Burnout will be assessed using the Maslach Burnout Inventory (MBI), a 22-item self-report scale measuring emotional exhaustion, depersonalization, and personal accomplishment. In this study, the personal accomplishment subscale will be reverse-coded so that higher total scores indicate higher levels of burnout. Scores range from 0 to 88. MBI is widely used to assess occupational burnout among healthcare professionals.
Baseline, immediately after the intervention (6 weeks), 1-month follow-up, and 3-month follow-up.
Secondary Outcomes (1)
Communication Skills (Communication Skills Scale for Health Professionals)
Baseline, immediately after the intervention (6 weeks), 1-month follow-up, and 3-month follow-up.
Study Arms (2)
Arm Title: Balint-Based Group Intervention
EXPERIMENTALParticipants in this arm received a Balint-based group intervention consisting of six weekly online sessions, each lasting 45-50 minutes. Sessions followed the structure recommended by the International Balint Federation, including case presentation, exploration, group discussion, feedback, and closing phases. The intervention was delivered by two psychiatric nursing academics trained in psychotherapy techniques. The group was conducted as a closed group, and sessions were scheduled according to nurses' shift patterns
Arm Title → Control Group (No Intervention)
NO INTERVENTIONParticipants in this arm continued their routine work schedules and did not receive any additional training, counseling, or psychosocial intervention during the study period. Data collection was performed at the same time points as the intervention group (baseline, post-intervention, 1-month follow-up, and 3-month follow-up). After the study was completed, the control group was informed about the intervention
Interventions
A Balint-based group intervention consisting of six weekly online sessions lasting 45-50 minutes. Sessions followed the structure recommended by the International Balint Federation, including case presentation, exploration, group discussion, feedback, and closing phases. The intervention was delivered by two psychiatric nursing academics trained in psychotherapy techniques. The group was conducted as a closed group, and sessions were scheduled according to participants' shift patterns
Eligibility Criteria
You may qualify if:
- having worked as a nurse in the same clinical setting for at least one year
- providing informed consent to participate
You may not qualify if:
- presence of a communication impairment that could hinder participation (e.g., hearing or speech disorder)
- Discontinuation Criteria:
- Voluntary withdrawal from the study
- Failure to attend at least two sessions
- Incomplete or missing data on the study instruments
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bilecik Şeyh Edebali University, Faculty of Health Sciences
Bilecik, Turkey (Türkiye)
Related Publications (1)
Huang L, Harsh J, Cui H, Wu J, Thai J, Zhang X, Cheng L, Wu W. A Randomized Controlled Trial of Balint Groups to Prevent Burnout Among Residents in China. Front Psychiatry. 2020 Feb 11;10:957. doi: 10.3389/fpsyt.2019.00957. eCollection 2019.
PMID: 32116808RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor of Psychiatric Nursing
Study Record Dates
First Submitted
November 28, 2025
First Posted
December 11, 2025
Study Start
December 20, 2024
Primary Completion
April 5, 2025
Study Completion
April 5, 2025
Last Updated
December 11, 2025
Record last verified: 2025-11
Data Sharing
- IPD Sharing
- Will not share