The Effect of the Educatıon and Counselıng of Prostatectomy Patıents
The Effect of educatıon and counselıng gıven to patıents patıent wıth Prostatectomy on qualıty of lıfe
1 other identifier
interventional
42
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable prostate-cancer
Started Jul 2022
Shorter than P25 for not_applicable prostate-cancer
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 15, 2022
CompletedFirst Posted
Study publicly available on registry
June 22, 2022
CompletedStudy Start
First participant enrolled
July 10, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 25, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
January 10, 2023
CompletedAugust 9, 2023
August 1, 2023
4 months
June 15, 2022
August 7, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
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.
six months
Study Arms (2)
experiment group
EXPERIMENTALIn 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.
control group
NO INTERVENTIONstandard care will be applied
Interventions
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cukurova University
Adana, 01030, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- lecturer Dr.
Study Record Dates
First Submitted
June 15, 2022
First Posted
June 22, 2022
Study Start
July 10, 2022
Primary Completion
October 25, 2022
Study Completion
January 10, 2023
Last Updated
August 9, 2023
Record last verified: 2023-08