Educatıon in Patıents Who Had Total Knee Prosthesıs

NCT06521073 | Not Yet Recruiting

• 1 other identifier: 06.01.2024/129
• Study Type: interventional
• Target: 60
• Locations: 0 countries
• Sites: N/A

Brief Summary

The main purposes of nursing care and education for patients who will undergo total knee prosthesis are; The aim is to reduce pain, prevent complications that may develop due to orthopedic surgery, increase patient satisfaction, and preserve function and mobilization.

Conditions

Prosthesis-Related Infections; Pain, Postoperative; Analgesia

Keywords

education; pain; Total Knee Prosthesis

Outcome Measures

Primary Outcomes (1)

• Primary Outcome Measure

  Patient Information Form (PIF) This form, prepared by scanning the literature, includes the patient's age, gender, marital status, education level, profession, social security, place of residence, presence of caregivers in the family, from whom he/she receives care, chronic diseases, the side on which knee prosthesis is applied, knee prosthesis. It is a form consisting of questions about your training status, who you received your training from, and your satisfaction with the training.

  1 week

Secondary Outcomes (1)

• Secondary Outcome Measures

  12 weeks

Other Outcomes (1)

• Third Outcome Measures

  12 weeks

Study Arms (2)

Experimental

EXPERIMENTAL

Before Surgery HBF ONE SAO Patient Education Material Post-Operation (1st, 2nd, 3rd day) ONE SAO Patient Education Material 10-14. BI and PSA will be applied on days and 6 weeks.

Behavioral: education

Control

NO INTERVENTION

Before Surgery HBF ONE SAO Routine verbal training of the clinic Post-Operation (1st, 2nd, 3rd day) ONE SAO Routine verbal training of the clinic 10-14. BI and PSA will be applied on days and 6 weeks.

Interventions

education BEHAVIORAL

Patient Information Form (HBF): This form, prepared by scanning the literature, includes the patient\'s age, gender, marital status, education level, profession, social security, place of residence, presence of caregivers in the family, from whom he/she receives care, chronic diseases, the side on which knee prosthesis is applied, knee prosthesis. It is a form consisting of questions about your training status, who you received your training from, and your satisfaction with the training. Barthel Index (BI): Barthel activities of daily living index is an evaluation scale used to measure an individual\'s performance in daily living activities. The index is used for activities of daily living in 10 domains. The Turkish validity and reliability of the Barthel index, developed by Barthel and Mahoney (1965), was determined by Küçükdeveci et al. (17).

Experimental

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• age over
• Being literate,
• Having knee replacement surgery for the first time;
• Not having chronic diseases or psychiatric diagnoses that would delay wound healing,
• Except hypertension;
• İt will include not developing any early complicationsthe research was planned to be carried out in three stages.

You may not qualify if:

• Hospitalized for at least 24 hours
• Agreeing to participate in the study

Sponsors & Collaborators

• Cukurova University: lead

MeSH Terms

Conditions

Prosthesis-Related Infections; Pain, Postoperative; Agnosia; Pain

Interventions

Educational Status

Condition Hierarchy (Ancestors)

Infections; Postoperative Complications; Pathologic Processes; Pathological Conditions, Signs and Symptoms; Neurologic Manifestations; Signs and Symptoms; Perceptual Disorders; Neurobehavioral Manifestations; Nervous System Diseases

Intervention Hierarchy (Ancestors)

Socioeconomic Factors; Population Characteristics

Study Officials

• sevban arslan

  Cukurova Universty

  STUDY DIRECTOR

Central Study Contacts

ilknur tura, MsC

CONTACT

+903223386084; itura@cu.edu.tr

sevban arslan, Phd

CONTACT

+903223386084; sarslan@cu.edu.tr

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Research Assistant

Study Record Dates

• First Submitted: June 14, 2024
• First Posted: July 25, 2024
• Study Start: September 1, 2024
• Primary Completion: September 1, 2024
• Study Completion: September 1, 2025
• Last Updated: July 25, 2024

Record last verified: 2024-07

Data Sharing

• IPD Sharing: Will not share