Back to resultsThe Effect of the Educatıon and Counselıng of Prostatectomy Patıents
Primary Purpose
Prostate Cancer, Surgery, Nursing Caries
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
education
Sponsored by
About this trial
This is an interventional supportive care trial for Prostate Cancer
Eligibility Criteria
Inclusion Criteria:
- Being 18 years or older,
- Being literate,
- Being able to understand and speak Turkish and not have a hearing impairment,
- Agreeing to participate in the research.
Exclusion Criteria:
- Development of any complications during the surgical intervention,
- Having any psychiatric disorder that will reduce the ability to comprehend and understand,
- Having other concomitant cancer,
- Having metastases.
Sites / Locations
- Cukurova University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
experiment group
control group
Arm Description
In addition to standard care, patients will be given discharge training, planned within the framework of the Life model, one day before discharge. It is planned that the discharge training will be given by the researcher in the patient's room and by providing an accompanying person. Written training material will be delivered to the patients for their re-use after the training.
standard care will be applied
Outcomes
Primary Outcome Measures
Effect of traınıng and counselıng gıven after prostatectomy on qualıty of lıfe
It will be measured with SF-12. Measurement will be made before and after the application. It is evaluated between 0 and 100 points, with a higher score representing better health.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05428098
Brief Title
The Effect of the Educatıon and Counselıng of Prostatectomy Patıents
Official Title
The Effect of educatıon and counselıng gıven to patıents patıent wıth Prostatectomy on qualıty of lıfe
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
July 10, 2022 (Actual)
Primary Completion Date
October 25, 2022 (Actual)
Study Completion Date
January 10, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cukurova University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The research was planned as a randomized controlled experimental study. This study is planned to be conducted in the Urology clinic of a university hospital located in the south of Turkey. The population of the research will be the patients admitted to the urology clinic for prostatectomy. The sample of the study will consist of patients who meet the criteria for participation in the study and volunteer to participate in the study. Evaluation of the research data will be done with the SPSS package program.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer, Surgery, Nursing Caries
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
42 (Actual)
8. Arms, Groups, and Interventions
Arm Title
experiment group
Arm Type
Experimental
Arm Description
In addition to standard care, patients will be given discharge training, planned within the framework of the Life model, one day before discharge. It is planned that the discharge training will be given by the researcher in the patient's room and by providing an accompanying person. Written training material will be delivered to the patients for their re-use after the training.
Arm Title
control group
Arm Type
No Intervention
Arm Description
standard care will be applied
Intervention Type
Other
Intervention Name(s)
education
Intervention Description
Oral and written education according to the life model
Primary Outcome Measure Information:
Title
Effect of traınıng and counselıng gıven after prostatectomy on qualıty of lıfe
Description
It will be measured with SF-12. Measurement will be made before and after the application. It is evaluated between 0 and 100 points, with a higher score representing better health.
Time Frame
six months
10. Eligibility
Sex
All
Gender Based
Yes
Gender Eligibility Description
Only male patients will be covered due to the surgical procedure.
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Being 18 years or older,
Being literate,
Being able to understand and speak Turkish and not have a hearing impairment,
Agreeing to participate in the research.
Exclusion Criteria:
Development of any complications during the surgical intervention,
Having any psychiatric disorder that will reduce the ability to comprehend and understand,
Having other concomitant cancer,
Having metastases.
Facility Information:
Facility Name
Cukurova University
City
Adana
ZIP/Postal Code
01030
Country
Turkey
12. IPD Sharing Statement
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The Effect of the Educatıon and Counselıng of Prostatectomy Patıents
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