A single centre, Prospective, Open-label, nonrandomized, interventional study to Evaluate the Impact of Emotional Intelligence Training and Management on Doctor–Patient Communication, Adherence, and Satisfaction in a Tertiary Care Hospital of District Thane, Maharashtra.
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 131
- 试验地点
- 1
研究概览
简要总结
This single-centre, prospective, open-label, non-randomized interventional study aims to evaluate the impact of Emotional Intelligence (EI) training on doctor–patient communication, treatment adherence, and patient satisfaction at a tertiary care hospital in Thane, Maharashtra. The study will enroll 84 doctors involved in direct patient care and 131 adult patients under their care. Doctors will undergo a structured EI training program focused on self-awareness, empathy, emotional regulation, interpersonal sensitivity, and communication skills, delivered through interactive sessions including case studies, role plays, and group discussions. Doctors’ EI levels (TEIQue-SF), patient satisfaction (PSQ-18), and treatment adherence will be assessed at baseline, 1 month, and 3 months post-training. Eligible participants include doctors with at least three years of clinical experience and patients aged 18 years or older capable of completing questionnaires, while participants with cognitive impairments, prior EI training, or conflicting study involvement are excluded. The study duration is six months. The primary endpoint is the change in doctors’ EI scores, and secondary endpoints include changes in patient treatment adherence and satisfaction. All adverse events and serious adverse events will be reported to the Ethics Committee, and participant confidentiality will be maintained.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 85.00 Year(s)(—)
- 性别
- All
入选标准
- •For Doctors: 1.Actively involved in direct patient care across various departments.
- •2.Minimum of more than 3 year of clinical experience post-qualification.
- •3.Willingness to participate in all phases of the study, including training and follow-up assessments.
- •4.Ability to understand and complete self-report questionnaires in the language of administration.
- •5.Provided informed consent.
- •For Patients: 1.Under the care of participating doctors during the study period.
- •2.Aged 18 years or older.
- •3.Capable of understanding and responding to the treatment adherence and satisfaction questionnaires.
- •4.Provided informed consent.
- •5.Available for follow-up assessments at designated time points.
排除标准
- •For Doctors: 1.Administrative or non-clinical roles with no direct patient interaction.
- •2.Prior formal training in emotional intelligence or communication skills within the last 12 months.
- •3.Unwilling or unable to attend the full training and reinforcement sessions.
- •4.Currently involved in another interventional study that may influence communication behaviour.
- •For Patients: 1.Cognitive impairments or psychiatric conditions that hinder reliable self-reporting.
- •2.Language barriers that prevent understanding of the questionnaire (unless translated versions are available).
- •3.Terminal illness or critical condition requiring intensive care.
研究者
Dr Ila Ghosh
Bhaktivedanta Hospital and Research Institute
