Pecha KukaNCT06339723
Pecha Kuka Method About Percutaneous Endoscopic Gastrostomy for Caregivers Who Care for Palliative Care Patients
A study testing Pecha Kucha in people with Pecha Kuka and Palliative Care, run by Firat University at 1 site in Turkey (Türkiye).
Trial summary
Palliative care; It was started by Dame Cicely Saunders in the 1960s as a hospice for community-based provision. Today, palliative care is defined as care that begins with the patient's diagnosis, symptom management is carried out effectively, and a comprehensive, supportive, humanistic approach is based on the… Read more about this study
- Who is it for?
- Ages 18 to 75 yearsHealthy volunteers can take part
- Conditions the study is for
- Pecha Kuka, Palliative Care
- What is being tested?
- Pecha Kucha
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 25 Feb 2024to 3 Jun 2024
- 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 18 to 75 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Accepting research
- Being a relative of a palliative care patient
- Ability to communicate adequately
Who cannot join
- The patient's relative has a disability (such as vision, speech and hearing) that prevents them from communicating.
- No psychiatric problems
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Examination of the Effectiveness of Training Given to Caregivers About Percutaneous Endoscopic Gastrostomy Using the Pecha Kuka Method to Caregivers Who Care for Palliative Care Patients
Palliative care; It was started by Dame Cicely Saunders in the 1960s as a hospice for community-based provision. Today, palliative care is defined as care that begins with the patient's diagnosis, symptom management is carried out effectively, and a comprehensive, supportive, humanistic approach is based on the individual and his family. When the literature was examined, no study was found that evaluated the effectiveness of the training given by the Pecha Kuka method to caregivers caring for palliative care patients about percutaneous endoscopic gastrostomy. In addition, it is thought that the results of this research will shed light on identifying problems related to feeding practices in patients fed with PEG tubes and identifying misinformation and practices of caregivers. Determining the knowledge level and initiatives of caregivers regarding percutaneous endoscopic gastrostomy tube feeding practices will contribute to the development of educational activities and effective strategies. Study results may provide important data regarding improving the quality of care given to patients and caregivers after discharge and controlling complication rates.
- Conditions
- Pecha Kuka, Palliative Care
- Being tested
- Pecha Kucha
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Pecha KuchaBehavioural
Pecha Kucha Method training was given
| Study group | Role | What they receive |
|---|---|---|
| Experimental | Experimental | Training Given with the Pecha Kucha Method Receives: Behavioral: Pecha Kucha |
| Control | No intervention | No training was given on the Pecha Kucha Method |
What is being measured
The primary outcome is the main question the study is designed to answer.
Evaluation Form for Feeding Practices with Percutaneous Endoscopic Gastrostomy Tube:
This data collection tool was created by researchers to evaluate the nutritional practices of individuals caring for patients fed through PEG tubes. Storage of the enteral nutrition product, duration of use after opening, dressing the feeding tube, rotating the plate 360 degrees during dressing, positioning the patient during feeding, checking the number written at the entrance of the feeding tube every time the nutritional product is given to the patient, use of nutritional products, duration of administration of the enteral nutrition product
Measured: 4 week
Visual Analog Scale -Anxiety:
Developed by Cline et al. It consists of a horizontal line 10 cm long. The left side contains the labels "no anxiety" and the right side includes the labels "I feel a lot of anxiety". The VAS value is determined by measuring the distance between the leftmost tip of the scale and the marked point. Values range from 0 to 10, with higher values indicating increased anxiety
Measured: 4 week
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Apr 2024
- Study start25 Feb 2024
- Primary completion13 Mar 2024
- Study completion3 Jun 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Pecha KukaStudies 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
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- Firat University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Gülcan Bahçecioğlu Turan, Firat University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06339723
- Sponsor's protocol ID
- 2024/03-17
- Status last verified
- Jun 2024
- First submitted
- 23 Feb 2024
- Last updated
- 11 Jun 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Erden Y, Karakurt N, Turan GB. Innovative Education in Palliative Care: Enhancing Caregiver Knowledge and Reducing Anxiety Through the Pecha Kucha Method for PEG Tube Feeding. Scand J Caring Sci. 2026 Jun;40(2):e70279. doi: 10.1111/scs.70279.
PubMed 42290120
Study at a glance
From the registry record, last updated by the sponsor on 11 Jun 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Examination of the Effectiveness of Training Given to Caregivers About Percutaneous Endoscopic Gastrostomy Using the Pecha Kuka Method to Caregivers Who Care for Palliative Care Patients
- ClinicalTrials.gov ID
- NCT06339723
- Acronym / sponsor ID
- 2024/03-17
- Conditions
- Pecha Kuka, Palliative Care
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Firat UniversityUniversity, hospital or other
- Study start
- 25 Feb 2024 (actual)
- Primary completion
- 13 Mar 2024 (actual)
- Study completion
- 3 Jun 2024 (actual)
- First posted
- 1 Apr 2024 (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.
Palliative care; It was started by Dame Cicely Saunders in the 1960s as a hospice for community-based provision. Today, palliative care is defined as care that begins with the patient's diagnosis, symptom management is carried out effectively, and a comprehensive, supportive, humanistic approach is based on the individual and his family. When the literature was examined, no study was found that evaluated the effectiveness of the training given by the Pecha Kuka method to caregivers caring for palliative care patients about percutaneous endoscopic gastrostomy. In addition, it is thought that the results of this research will shed light on identifying problems related to feeding practices in patients fed with PEG tubes and identifying misinformation and practices of caregivers. Determining the knowledge level and initiatives of caregivers regarding percutaneous endoscopic gastrostomy tube feeding practices will contribute to the development of educational activities and effective strategies. Study results may provide important data regarding improving the quality of care given to patients and caregivers after discharge and controlling complication rates.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Experimental | Experimental | Behavioral: Pecha KuchaTraining Given with the Pecha Kucha Method |
| Control | No intervention | –No training was given on the Pecha Kucha Method |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Accepting research
- Being a relative of a palliative care patient
- Ability to communicate adequately
Key exclusion criteria (2 listed)
- The patient's relative has a disability (such as vision, speech and hearing) that prevents them from communicating.
- No psychiatric problems
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 |
|---|---|---|
| Pecha KuchaPecha Kucha Method training was given | Behavioural | Experimental |
Primary outcome
Evaluation Form for Feeding Practices with Percutaneous Endoscopic Gastrostomy Tube:
Time frame: 4 week
This data collection tool was created by researchers to evaluate the nutritional practices of individuals caring for patients fed through PEG tubes. Storage of the enteral nutrition product, duration of use after opening, dressing the feeding tube, rotating the plate 360 degrees during dressing, positioning the patient during feeding, checking the number written at the entrance of the feeding tube every time the nutritional product is given to the patient, use of nutritional products, duration of administration of the enteral nutrition product
Visual Analog Scale -Anxiety:
Time frame: 4 week
Developed by Cline et al. It consists of a horizontal line 10 cm long. The left side contains the labels "no anxiety" and the right side includes the labels "I feel a lot of anxiety". The VAS value is determined by measuring the distance between the leftmost tip of the scale and the marked point. Values range from 0 to 10, with higher values indicating increased anxiety
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 11 Jun 2024.
- Derived from this study: PubMed 42290120Erden Y, Karakurt N, Turan GB. Innovative Education in Palliative Care: Enhancing Caregiver Knowledge and Reducing Anxiety Through the Pecha Kucha Method for PEG Tube Feeding. Scand J Caring Sci. 2026 Jun;40(2):e70279. doi: 10.1111/scs.70279.
- Individual participant dataSharing planned: No
Related trials for Pecha Kuka
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 Pecha Kucha in people with Pecha Kuka and Palliative Care, run by Firat University 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 3 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 11 Jun 2024. 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?
Evaluation Form for Feeding Practices with Percutaneous Endoscopic Gastrostomy Tube: (time frame: 4 week). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06339723, which also lists 1 linked publication.
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 11 Jun 2024.