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Clinical Trials/NCT04916717
NCT04916717
Completed
Not Applicable

Effect Of Counselıng on Qualıty of Lıfe and Self-Care Agency for Patıents Who Are Scheduled for Total Knee Replacement

Uşak University1 site in 1 country79 target enrollmentApril 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Total Knee Replacement
Sponsor
Uşak University
Enrollment
79
Locations
1
Primary Endpoint
Quality of life (SF-36)
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This study aims to determine the effect of counseling on quality of life and self-care agency for patients who are scheduled for TKR.

Detailed Description

This is a quantitative study and has a quasi-experimental design with a control group. The sample of the study consisted of 79 patients including intervention (n=39) and control (n=40). The data are collected by the face-to-face interview method using Patient Identification Form, Quality of Life Scale, and Self-Care Agency Scale before surgery, and 6-8th weeks after discharge. Face-to-face and telephone counseling were applied to individuals in the intervention group. The x2, t-test, one-factor variance analysis, and two-factor variance analysis were used in the analysis of the data.

Registry
clinicaltrials.gov
Start Date
April 1, 2018
End Date
December 31, 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Sponsor
Uşak University
Responsible Party
Principal Investigator
Principal Investigator

çiğdem kaya

Lecturer, PhD

Uşak University

Eligibility Criteria

Inclusion Criteria

  • undergoing TKA for the first time, being scheduled to have unilateral TKA, having surgery for osteoarthritis, having no postoperative complications, fulfilment of discharge criteria after surgery, being aged 18 years or older, being conscious, orientation to place and time, having no hearing or speech problems, ability to understand and speak Turkish, being at least literate, not being diagnosed with any psychiatric diseases and not having a history of cancer.

Exclusion Criteria

  • diagnoses of neurological (e.g. Alzheimer's disease) and psychiatric disorders (e.g. schizophrenia) likely to affect cognitive functions, first accepting to participate in the study and then dropping out of the study, development of complications during follow-up (e.g. infection), unavailability when called and lost to follow-up.

Outcomes

Primary Outcomes

Quality of life (SF-36)

Time Frame: up to 16 weeks

in quality of life change from the preoperative period to 6-8th weeks and 14-16th weeks (postoerative period)

Self Care Agency

Time Frame: up to16 weeks

in self care agency change from the preoperative period to 6-8th weeks and 14-16th weeks (postoerative period)

Study Sites (1)

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