The Impact of Chatbot-Assisted Nursing Education on Perceived Burden of Care and Caregiver Stress
NCT ID: NCT06544421
Last Updated: 2024-08-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
62 participants
INTERVENTIONAL
2024-08-10
2025-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Impact of ChatGPT-based Nursing Process Training
NCT06297382
The Effect of Conscious Awareness Development Psychoeducation Program Prepared for Caregivers
NCT06675773
Nurses' Attitudes Toward Artificial Intelligence and Their Relationship With Critical Thinking Dispositions
NCT07134374
Nursing Students' Attitudes Towards Artificial Intelligence and Exam Anxiety Levels
NCT06217926
AI-Powered Interview Simulation to Improve Employability and Reduce Anxiety in Nursing and Midwifery Students
NCT07061132
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The caregivers included in the experimental group will be told about the study and their written consent will be obtained. Individuals in the experimental group will be asked to apply the data collection forms prepared before the use of the application is explained. After the pre-test data is collected, a chatbot-supported application will be installed on the caregivers in the experimental group. In order for them to participate in the sessions and complete the trainings in the determined plan flow, caregivers will be called by phone and reminders will be made and checked. The sessions are expected to end in 4 weeks (8 sessions) (Gabrielli et al., 2021).A participant will be scheduled to finish the application within a maximum of 4 weeks. No intervention will be applied to the control group, they will be followed up within the scope of the routine follow-up and treatment protocol of the clinic. The chatbot-supported application, which will be prepared for stroke patient care providers, has been prepared in line with the literature using the COM-B model according to the needs of caregivers. The prepared training content was sent to the experts and the final shape was given by taking the opinions of the experts
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1 week : What is Stroke, Taking Care of the Individual with Physical Needs-1
Session 1 What is Stroke, The Importance of Post-Stroke Rehabilitation, Obtaining accurate health information, Contacting the Health Team, Difficult caregiving behaviors Support mechanisms in stroke patient care
Assigned Interventions
Assigned Interventions
Week 1: What is a Stroke, Caring for Someone with Physical Needs-2
Session 2 Personal Care, Prevent pressure sores Position and handling techniques Pain In-bed exercises Self-care Nutrition Sleep Speech \& Communication Medication Management Emotional and Cognitive Changes in the Stroke Individual
Assigned Interventions
Assigned Interventions
Week 2: Stress of Care, Becoming resistant to stress Coping with stress-1
Session 1 Caregiving role barriers and facilitators Positive Aspects of Caregiving Care Stress and Its Causes, Reaction to Stress Maintaining emotional balance in the caregiving process
Assigned Interventions
Assigned Interventions
Week 2: Stress of Care, Becoming resistant to stress Coping with stress-2
Self-knowledge and motivation Maintenance and Time Management Controlling the Body in the Caregiving Process Breathing and relaxation
Assigned Interventions
Assigned Interventions
Week 3: Supporting oneself in the caregiving process and becoming resistant to stress-1
Session 1:
Personal space and comfort in the care process Taking time for yourself Unreasonable beliefs and mental regulation technique Tackling anxieties
Assigned Interventions
Assigned Interventions
Week 3: Supporting oneself in the caregiving process and becoming resistant to stress-2
The importance of nutrition The importance of physical activity Regulation of sleep
Assigned Interventions
Assigned Interventions
4 week: Control of emotions and spirituality in the process of care-1
Anger management Unleashing emotions and social relationships Use of humor
Assigned Interventions
Assigned Interventions
4 week: Control of emotions and spirituality in the process of care-2
Communication and Empathy Spirituality and religious coping Pray Be happy
Assigned Interventions
Assigned Interventions
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Assigned Interventions
Assigned Interventions
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Caregivers have the cognitive capacity to use chatbots (The chatbot application will be installed on the caregiver's android phone and the status of using it will be evaluated)
* Willingness to participate in the study
* To be open to communication and cooperation
* Having a phone with Android operating system
* Have literacy skills
* Not having participated in stress training before
Exclusion Criteria
* Taking antipsychotic medication
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ataturk University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Esra Yılmaz Bayrakçeken
Esra Yılmaz Bayrakçeken
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
esrabayrakceken1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.