Effect Of Counselıng

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

79 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-04-01

Study Completion Date

2019-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Investıgatıon Of The Effect Of Traınıng And Counselıng Provıded By Tele Nursing

NCT06130098

Musculoskeletal Diseases

NOT_YET_RECRUITING NA

The Effect of Health Promotion Training on Life Qualities and Self-Care Powers in Stroke Patients

NCT05484843

Stroke Nursing Caries Quality of Life +1 more

COMPLETED NA

The Effect of Tele-Consultation Supported Education After Total Knee Arthroplasty Surgery

NCT06784596

Knee Arthroplasty, Total

NOT_YET_RECRUITING NA

The Effect of Telephone Nursing Education and Counseling Services Given to Satisfaction Level and Self-Care Strength

NCT05487638

Postoperative Complications

COMPLETED NA

The Effect of the Educational Plan Prepared According to the Health Literacy Levels of Patients

NCT05088551

Total Knee Arthroplasty Patient Education

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Total Knee Replacement Quality of Life Nursing Caries

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SEQUENTIAL

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

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Counseling

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

Group Type OTHER

Counseling

Intervention Type OTHER

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

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Counseling

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

Intervention Type OTHER

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Patient education

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.

Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes