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Effect Of Counselıng

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04916717
Enrollment
79
Registered
2021-06-07
Start date
2018-04-01
Completion date
2019-12-31
Last updated
2021-06-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nursing Caries, Quality of Life, Total Knee Replacement

Keywords

total knee replacement, nursing counseling, counseling, quality of life, self care agency

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.

Interventions

OTHERCounseling

Face-to-face and telephone counseling were applied to individuals in the intervention group.

Sponsors

Uşak University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

This is a quantitative study and has a quasi-experimental design with a control group.

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Quality of life (SF-36)up to 16 weeksin quality of life change from the preoperative period to 6-8th weeks and 14-16th weeks (postoerative period)
Self Care Agencyup to16 weeksin self care agency change from the preoperative period to 6-8th weeks and 14-16th weeks (postoerative period)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026