SurgeryNCT06928025
Effectiveness of Animation-Based Education Given to Elderly Patients Undergoing Coronary Artery Bypass Graft Surgery
A study testing Preoperative Education in people with Surgery, run by Ayşegül Sena Pirgaip Yavuz at 1 site in Turkey (Türkiye).
Trial summary
It was conducted to measure the effectiveness of animation-based training given to elderly patients who will undergo coronary artery bypass graft surgery on the patients' pain, fear, anxiety and self-care management. The study will be completed with 72 participants, 35 experimental and 37 control. Read more about this study
- Who is it for?
- Ages 65 years and olderHealthy volunteers can take part
- Conditions the study is for
- Surgery
- What is being tested?
- Preoperative Education
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 72 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Apr 2023to 24 Jan 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 65 years and older
- All sexes
- Healthy volunteers accepted
- Older adult
Who may be able to join
- 65 years of age or older,
- No diagnosed functional disability,
- First scheduled coronary artery bypass graft surgery,
- Those who volunteered to participate in the study
Who cannot join
- Urgent cases,
- Cases with additional surgical procedures
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Effectiveness of Animation-Based Training Given to Elderly Patients Who Will Have Coronary Artery Bypass Graft Surgery on Their Pain, Fear, Anxiety and Self-Care Management: Randomized Control Study
It was conducted to measure the effectiveness of animation-based training given to elderly patients who will undergo coronary artery bypass graft surgery on the patients' pain, fear, anxiety and self-care management.
The study will be completed with 72 participants, 35 experimental and 37 control.
Read more
As a randomization method, simple randomization method will be used to ensure equal number of samples in the two groups, and patients will be verbally informed about the study and written informed consent will be obtained from the patients who agree.
In this study, the effectiveness of animation-based training given to elderly patients undergoing coronary artery bypass graft surgery on pain, fear, anxiety and self-care management will be evaluated.
Read the detailed description
Experimental: Patients in the experimental group will be given animation-based video training with a laptop one day before the surgery. The animation-based video training lasts 8 minutes and 35 seconds in total.
Patient Information Form, Self-Care Management in Chronic Diseases Scale, Visual Analog Scale, Hospital Anxiety Depression Scale, Surgical Fear Scale (Turkish Version) will be applied.
Control: In the preoperative period, no training will be given by the researcher to the patients constituting the control group. Patients in this group will receive the routine training of the clinic before surgery. Patient Information Form, Self-Care Management in Chronic Diseases Scale, Visual Analog Scale, Hospital Anxiety Depression Scale, Surgical Fear Scale (Turkish Version) will be applied.
- Conditions
- Surgery
- Being tested
- Preoperative Education
- Keywords
- Nursing, elderly patient, anxiety, self-care management, pain, fear, coronary artery bypass surgery
- Medical subject headings
- Anxiety Disorders, Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Preoperative EducationProcedure or surgery
animation-based education for elderly patients before coronary artery bypass graft surgery Before coronary artery bypass graft surgery, the scenario prepared based on the literature information including introduction of the service, preparation for surgery, monitoring, drug treatment and applications, deep breathing and cough exercise, spirometer use, operation time, postoperative period and care, patient pain management and intubation process will be given as animation-based video training. The effects of this on postoperative pain, fear, anxiety and self-care management will be evaluated.
| Study group | Role | What they receive |
|---|---|---|
| Animation Based Education | Experimental | Experimental: Patients in the experimental group will be given animation-based video training with a laptop one day before the surgery. The animation-based video training lasts 8 minutes and 35 seconds in total.
Patient Information Form, Self-Care Management in Chronic Diseases Scale, Visual Analog Scale, Hospital Anxiety Depression Scale, Surgical Fear Scale (Turkish Version) will be applied. Receives: Procedure: Preoperative Education |
| Control | No intervention | Control: In the preoperative period, no training will be given by the researcher to the patients constituting the control group. Patients in this group will receive the routine training of the clinic before surgery. Patient Information Form, Self-Care Management in Chronic Diseases Scale, Visual Analog Scale, Hospital Anxiety Depression Scale, Surgical Fear Scale (Turkish Version) will be applied. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Patient Information Form
The personal information form used for data collection consists of demographic characteristics of the individuals such as age, gender, marital status, occupation, educational status, employment status, as well as questions including health-related conditions of the patients such as chronic diseases, whether they have had surgery before or not.
Measured: Up to 24 weeks
Secondary outcomes (1)
Self-Care Management Scale in Chronic Diseases
Self-Care Management-Protection (SCMP-G) After Jones and Preuett defined the concept of self-care management process (SCMP), the validity of SCMP was tested and the characteristics of the protection concept were explained and added.While developing the SCMP-G scale, two types of protection concepts were defined.These concepts were determined as self-protection and social protection and formed two sub-dimensions of the scale. The self-protection sub-dimension consists of items numbered 2, 6, 8, 11, 15, 18, 19, 20, 22, 23 and 25-34, while the social protection sub-dimension consists of items numbered 1, 3-5, 7, 9, 10, 12-14, 16, 17, 21, 24 and 35.The scale has a format that is evaluated between 5 (Strongly Agree) and 1 (Strongly Disagree).The higher the score, the higher the level of self-care management.The Cronbach's Alpha of the self-care management scale in chronic patients is 0.85. The Cronbach's Alpha for this study was 0.89.
Measured: Up to 24 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Apr 2025
- Study start1 Apr 2023
- Primary completion1 Feb 2024
- Study completion24 Jan 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SurgeryStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 72 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ayşegül Sena Pirgaip Yavuz
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Ayşegül Sena Pirgaip Yavuz, Ataturk University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06928025
- Sponsor's protocol ID
- AYavuz
- Status last verified
- Apr 2025
- First submitted
- 30 Mar 2025
- Last updated
- 15 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 15 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effectiveness of Animation-Based Training Given to Elderly Patients Who Will Have Coronary Artery Bypass Graft Surgery on Their Pain, Fear, Anxiety and Self-Care Management: Randomized Control Study
- ClinicalTrials.gov ID
- NCT06928025
- Acronym / sponsor ID
- AYavuz
- Conditions
- Surgery
- Keywords
- Nursing, elderly patient, anxiety, self-care management, pain, fear, coronary artery bypass surgery
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 72 participants (actual)
- Lead sponsor
- Ayşegül Sena Pirgaip YavuzUniversity, hospital or other
- Study start
- 1 Apr 2023 (actual)
- Primary completion
- 1 Feb 2024 (actual)
- Study completion
- 24 Jan 2025 (actual)
- First posted
- 15 Apr 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
It was conducted to measure the effectiveness of animation-based training given to elderly patients who will undergo coronary artery bypass graft surgery on the patients' pain, fear, anxiety and self-care management.
The study will be completed with 72 participants, 35 experimental and 37 control.
As a randomization method, simple randomization method will be used to ensure equal number of samples in the two groups, and patients will be verbally informed about the study and written informed consent will be obtained from the patients who agree.
In this study, the effectiveness of animation-based training given to elderly patients undergoing coronary artery bypass graft surgery on pain, fear, anxiety and self-care management will be evaluated.
Detailed description
Experimental: Patients in the experimental group will be given animation-based video training with a laptop one day before the surgery. The animation-based video training lasts 8 minutes and 35 seconds in total.
Patient Information Form, Self-Care Management in Chronic Diseases Scale, Visual Analog Scale, Hospital Anxiety Depression Scale, Surgical Fear Scale (Turkish Version) will be applied.
Control: In the preoperative period, no training will be given by the researcher to the patients constituting the control group. Patients in this group will receive the routine training of the clinic before surgery. Patient Information Form, Self-Care Management in Chronic Diseases Scale, Visual Analog Scale, Hospital Anxiety Depression Scale, Surgical Fear Scale (Turkish Version) will be applied.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Animation Based Education | Experimental | Procedure: Preoperative EducationExperimental: Patients in the experimental group will be given animation-based video training with a laptop one day before the surgery. The animation-based video training lasts 8 minutes and 35 seconds in total. Patient Information Form, Self-Care Management in Chronic Diseases Scale, Visual Analog Scale, Hospital Anxiety Depression Scale, Surgical Fear Scale (Turkish Version) will be applied. |
| Control | No intervention | –Control: In the preoperative period, no training will be given by the researcher to the patients constituting the control group. Patients in this group will receive the routine training of the clinic before surgery. Patient Information Form, Self-Care Management in Chronic Diseases Scale, Visual Analog Scale, Hospital Anxiety Depression Scale, Surgical Fear Scale (Turkish Version) will be applied. |
Who may qualify
- Ages
- 65 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Older adult
Key inclusion criteria (4 listed)
- 65 years of age or older,
- No diagnosed functional disability,
- First scheduled coronary artery bypass graft surgery,
- Those who volunteered to participate in the study
Key exclusion criteria (2 listed)
- Urgent cases,
- Cases with additional surgical procedures
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Preoperative Educationanimation-based education for elderly patients before coronary artery bypass graft surgery Before coronary artery bypass graft surgery, the scenario prepared based on the literature information including introduction of the service, preparation for surgery, monitoring, drug treatment and applications, deep breathing and cough exercise, spirometer use, operation time, postoperative period and care, patient pain management and intubation process will be given as animation-based video training. The effects of this on postoperative pain, fear, anxiety and self-care management will be evaluated. | Procedure or surgery | Animation Based Education |
Primary outcome
Patient Information Form
Time frame: Up to 24 weeks
The personal information form used for data collection consists of demographic characteristics of the individuals such as age, gender, marital status, occupation, educational status, employment status, as well as questions including health-related conditions of the patients such as chronic diseases, whether they have had surgery before or not.
1 secondary outcome
Self-Care Management Scale in Chronic Diseases
Time frame: Up to 24 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Apr 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Preoperative Education in people with Surgery, run by Ayşegül Sena Pirgaip Yavuz at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 15 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Patient Information Form (time frame: Up to 24 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Apr 2025.