SYMPTOM MANAGEMENT EDUCATION GIVEN WITH MICRO TEACHING METHOD ENRICHED WITH STANDARD PATIENT IN PALLIATIVE CARE

• ClinicalTrials.gov Identifier: NCT05842226
• Recruitment Status: Recruiting
• First Posted: May 3, 2023
• Last Update Posted: May 3, 2023
• Sponsor: Ankara Yildirim Beyazıt University
• Information provided by (Responsible Party): Ankara Yildirim Beyazıt University

Tracking Information

• First Submitted Date: April 24, 2023
• First Posted Date: May 3, 2023
• Last Update Posted Date: May 3, 2023
• Actual Study Start Date: April 17, 2023
• Estimated Primary Completion Date: May 1, 2023 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: April 24, 2023)

• KNOWLEDGE LEVEL [ Time Frame: 2 months ]
  A knowledge test on symptom management and communication in palliative care was developed by the researcher. It consists of 25 questions.
• REFLECTIVE THINKING LEVEL [ Time Frame: 2 months ]
  Scale for Determining the Level of Reflective Thinking will be used. It is a 16-item 5-point Likert-type scale consisting of four sub-dimensions. Its sub-dimensions are habituation, comprehension, reflection and critical reflection.
• THERAPEUTIC COMMUNICATION SKILLS [ Time Frame: 2 months ]
  Therapeutic Communication Skills Scale for Nursing Students will be used. It is a 7-point Likert scale consisting of a total of 16 items, including 7 items in the NonTherapeutic Communication Skills sub-dimension, 6 items in the Therapeutic Communication Skills 1 sub-dimension, and 3 items in the Therapeutic Communication Skills 2 sub-dimension.

• Original Primary Outcome Measures: Same as current
• Change History: No Changes Posted

Current Secondary Outcome Measures (submitted: April 24, 2023)

• Micro Teaching Group Evaluation Form [ Time Frame: 2 weeks ]
  It was created by the researcher. It will be used for self-assessment by experts, peers and the student during the implementation.
• Standard Patient Evaluation Form [ Time Frame: 2 weeks ]
  Created by the researcher. It will be filled in by specialists during standardized patient practice.

• Original Secondary Outcome Measures: Same as current
• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: SYMPTOM MANAGEMENT EDUCATION GIVEN WITH MICRO TEACHING METHOD ENRICHED WITH STANDARD PATIENT IN PALLIATIVE CARE
• Official Title: THE EFFECT OF SYMPTOM MANAGEMENT EDUCATION GIVEN WITH MICRO TEACHING METHOD ENRICHED WITH STANDARD PATIENT IN PALLIATIVE CARE ON NURSING STUDENTS' KNOWLEDGE LEVEL, REFLECTIVE THINKING LEVEL AND THERAPEUTIC COMMUNICATION SKILLS
• Brief Summary: The study was planned as a randomized controlled pre-test, post-test intervention study to determine the effect of symptom management training in palliative care given with micro-teaching method enriched with standard patient on nursing students' knowledge levels, reflective thinking levels and therapeutic communication skills related to palliative care.
• Detailed Description: Sample of study was calculated as 36 using G*Power Software (ver. 3.1.9.2) for 80% power and medium effect size (f=0.40) at 95% confidence level in line with the data of Lin et al. The experimental and control groups were planned as 20 students each with a 10 percent loss. Participants were assigned to the experimental and control groups by the stratified randomization method. The locks were assigned to layers using Microsoft Excel. A pre-test will be applied to both groups. The control group will receive palliative care brochure for patients and their relatives.The practice group will be shared the 4 most common symptoms in palliative care nursing: pain, fatigue, respiratory distress and loss of appetite. The practice group will be 5 groups and there will be 4 students in each group. During the practice, each student will provide patient education about only one symptom. The standard patient will participate in the intervention in the application laboratory and the students will participate in the intervention in the computer environment. Video recordings will be taken while the students are giving education. After watching the experts, peers and their own video with the micro-teaching group evaluation form, the student himself/herself will make an evaluation. At the same time, a lecturer from outside the research will fill in the Standard Patient Check-List Evaluation Form. The application will be repeated one week later. After all the applications, the students will watch the video of their own 2 more times and the post-test will be applied to both groups. After one month, a retention test will be applied to the students in both groups.
• Study Type: Interventional
• Study Phase: Not Applicable
• Study Design: Allocation: Randomized; Intervention Model: Parallel Assignment; Masking: None (Open Label); Primary Purpose: Supportive Care
• Condition: Palliative Care

Intervention

Other: Micro-teaching enriched with standard patient

The practice group will be shared the 4 most common symptoms in palliative care nursing: pain, fatigue, respiratory distress and loss of appetite. The practice group will be 5 groups and there will be 4 students in each group. During the practice, each student will provide patient education about only one symptom. The standard patient will participate in the intervention in the application laboratory and the students will participate in the intervention in the computer environment. Video recordings will be taken while the students are giving education. After watching the experts, peers and their own video with the micro-teaching group evaluation form, the student himself/herself will make an evaluation. At the same time, a lecturer from outside the research will fill in the Standard Patient Check-List Evaluation Form. The application will be repeated one week later.

Study Arms

• Experimental: Intervention group
  Micro-teaching enriched with standard patient will be applied.
  Intervention: Other: Micro-teaching enriched with standard patient
• No Intervention: Control group
  The control group will receive palliative care brochure for patients and their relatives.

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Recruiting
• Estimated Enrollment (submitted: April 24, 2023): 40
• Original Estimated Enrollment: Same as current
• Estimated Study Completion Date: July 1, 2023
• Estimated Primary Completion Date: May 1, 2023 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• Students taking palliative care course for the first time,
• Students who agreed to participate in the study,

Exclusion Criteria:

• Students who have already taken the palliative care course,
• Students who answered the data collection forms incompletely,
• Students who do not want to continue the research,
• Students who missed even one of the theoretical or practical sessions of the study.
• Students with experience of caring for a palliative care patient

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 18 Years to 50 Years (Adult)
• Accepts Healthy Volunteers: Yes

Contacts

Contact: Esra Tayaz, phd; 05078106288; esratayaz@gmail.com

• Listed Location Countries: Turkey

Administrative Information

• NCT Number: NCT05842226
• Other Study ID Numbers: 2023-06
• Has Data Monitoring Committee: No

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

IPD Sharing Statement

• Plan to Share IPD: No

• Current Responsible Party: Ankara Yildirim Beyazıt University
• Original Responsible Party: Same as current
• Current Study Sponsor: Ankara Yildirim Beyazıt University
• Original Study Sponsor: Same as current
• Collaborators: Not Provided
• Investigators: Not Provided
• PRS Account: Ankara Yildirim Beyazıt University
• Verification Date: April 2023