- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06213441
Improving the Quality of Life and Self-sufficiency of Individuals With Stoma: Pecha Kucha Training Via Smartphone
Study Overview
Detailed Description
Colorectal cancers are the most common type of cancer among the top ten cancers, according to the 2020 Global Cancer Statistics. It also ranks third in terms of incidence and second in terms of mortality rate. Colorectal cancer is one of the most common cancer types in our country. It is also noteworthy that it is the 3rd most common cancer in both men and women Nowadays, the number of individuals who undergo stoma surgery due to colorectal cancer and other reasons and continue their lives with a stoma is increasing Pecha kucha (PK) is an innovative form of presentation used around the world . PK, derived from the Japanese word meaning "chat", helps present creative works with visual images . Pecha kucha is a compact and effective presentation method consisting of 20 slides, each presented in 20 seconds .This "20×20" format, which requires careful editing and develops the use of critical communication skills, serves as an innovative and valuable tool that allows the presenter to dynamically and systematically present important information worth sharing to the audience . Thanks to Pecha Kucha, the presenter conveys the topic quickly and clearly without deviating from the essence of the topic .PK may be superior to traditional PowerPoint presentations in terms of learning function. PK is as effective as traditional PowerPoint presentations in retaining information. It is stated that with the pecha kucha method, information can be presented in a more concise way, without any difference in quality, compared to a longer PowerPoint presentation PK presentation, including visual and narrative presentation, does not take more than 7-8 minutes Mobile phones, one of the technological developments today, are also equipped with information and communication servicesQuick applications using the phone in the postoperative period are an effective method for reducing anxiety and improving the quality of life and are used for this purpose It is stated in the literature that trainings that include the technology-supported role of nurses can significantly contribute to the quality of life, adaptation and competence of individuals in the stoma care process Strategic methods that use technology for patient compliance and competence, especially for stoma care, can be easily adapted to patients. the education given to patients with intestinal stomas via multimedia was associated with a higher level of compliance compared to face-to-face teaching. In the literature, there is a lack of studies examining the effect of stoma care education given to patients via mobile phone using the Pecha Kucha method on the quality of life and competence of patients.
Criteria for inclusion in the study Individuals who have had a stoma for the first time, who can speak and understand Turkish, who are literate and who volunteer to participate in the study will be included in the sample of the study.
Criteria for exclusion from the study Individuals who have previously had a stoma, who have difficulty speaking and understanding Turkish, and who do not approve of participating in the study will not be included in the sample of the study.
Exclusion criteria after the study begins Once the research begins, the participant can exit the research at any stage he/she wishes.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: MAİDE YEŞİLYURT
- Phone Number: +905378777581
- Email: md91yesilyurt@gmail.com
Study Locations
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-
-
Aksaray, Turkey (Türkiye)
- Recruiting
- Aksaray University
-
Contact:
- MAİDE YEŞİLYURT
- Phone Number: +905378777581
- Email: md91yesilyurt@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Having a stoma for the first time,
- Can speak Turkish,
- Can understand Turkish,
Exclusion Criteria:
- A stoma has been opened before,
- Having difficulty in speaking Turkish
- Having difficulty in understanding Turkish
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: arm trained with pecha kucha
The interventions to be applied to the experimental arm were as follows: a descriptive characteristics form was administered to the patient before discharge from the clinic.
The PC education presentation was shown to the patient via mobile phone before leaving the clinic and was also shared via WhatsApp using the phone numbers they used.
The PC education presentation lasted approximately 5-7 minutes.
Four weeks after the training, the Stoma Quality of Life Scale and the Stoma Self-Efficacy Scale were completed via an online survey.
|
Pecha kucha training to be given to the experimental arm will be given by the researcher. The training content will be created in line with the literature and will be given before the patient is discharged. |
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No Intervention: control arm
TInterventions to be applied to the control arm: A descriptive characteristics form was administered to the patient before discharge from the clinic.
Routine training was provided by the wound and stoma care nurse before discharge.
Four weeks after discharge, the patient was administered the Stoma Quality of Life Scale and the Stoma Self-Efficacy Scale via an online survey.
The study's implementation plan is outlined in Figure 1.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
LIFE QUALITY
Time Frame: 4 weeks later
|
Quality of life with stoma may change with pecha kucha training.
Stoma Quality of Life Scale was developed by Baxter et al., (2006) in 2006, and its Turkish validity and reliability study was conducted by Karadağ et al. in 2011.
(2011) is a 19-item scale.
The scale includes "Work and Social Life" (questions 3, 4, 5, 6, 18 and 19), "Sexual Life and Body Image" (questions 7, 8, 9, 12 and 15) and "Stoma Functions" (questions 10).
It has three sub-dimensions: questions 11, 13, 14, 16 and 17).
The first 2 questions of the scale are answered with a rating consisting of numbers between 0 and 100, which includes general satisfaction evaluation (0: complete dissatisfaction, 100: complete satisfaction).
|
4 weeks later
|
|
STOM SELF-EFFICIENCY
Time Frame: 4 weeks later
|
patients self-efficacy with stoma may change with pecha kucha training.
Stoma Self-Efficacy Scale was developed by Bekkers et al., (1996) in 1996, and its Turkish validity and reliability study was published by Karaçay et al. in 2020.
(2020) is a 22-item 5-point Likert type scale with 1 (I definitely do not trust), 2 (I have some confidence), 3 (I have sufficient confidence), 4 (I have a lot of confidence), 5 (I definitely trust).
The scale has two subscales: Stoma Care Self-efficacy (1-13 items) and Social Self-efficacy (14-22 items).
The scale is evaluated based on the total score.
The lowest score that can be obtained from the scale is 22, the highest score is 110, and higher scores indicate better self-efficacy levels.
Cronbach's alpha number of the scale was calculated as 0.95.
|
4 weeks later
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: MAİDE YEŞİLYURT, Aksaray University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- MYesilyurt2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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