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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05428098
Other study ID # 5312256941
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 10, 2022
Est. completion date January 10, 2023

Study information

Verified date August 2023
Source Cukurova University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date January 10, 2023
Est. primary completion date October 25, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
education
Oral and written education according to the life model

Locations

Country Name City State
Turkey Cukurova University Adana

Sponsors (1)

Lead Sponsor Collaborator
Cukurova University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Effect of training and counseling given after prostatectomy on quality of life 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
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