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Clinical Trials/NCT05428098
NCT05428098CompletedNot Applicable

The Effect of educatıon and counselıng gıven to patıents patıent wıth Prostatectomy on qualıty of lıfe

Cukurova University1 site in 1 country42 target enrollmentStarted: July 10, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
42
Locations
1
Primary Endpoint
Effect of traınıng and counselıng gıven after prostatectomy on qualıty of lıfe

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Supportive Care
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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.

Arms & Interventions

experiment group

Experimental

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.

Intervention: education (Other)

control group

No Intervention

standard care will be applied

Outcomes

Primary Outcomes

Effect of traınıng and counselıng gıven after prostatectomy on qualıty of lıfe

Time Frame: six months

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 Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sevgi Deniz Dogan

lecturer Dr.

Cukurova University

Study Sites (1)

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