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The Effect of Rehabilitative Nursing Care Practices on Frail Patients Undergoing Knee Arthroplasty and Their Caregivers

A

Ataturk University

Status

Not yet enrolling

Conditions

Knee Arthroplasty

Treatments

Behavioral: nursing care

Study type

Interventional

Funder types

Other

Identifiers

NCT07201454
Ilknaz_Doktara_Tezi

Details and patient eligibility

About

This study was designed to holistically examine the effects of curative nursing care practices based on human caring theory on frail patients and their caregivers undergoing knee arthroplasty.

Full description

Objective: This study was designed to thoroughly examine the effects of rehabilitative care practices based on the Human Caring Theory on the feeling of entrapment and caregiver burden of frail patients undergoing knee arthroplasty, as well as their impact on patient satisfaction.

Method: This study will be conducted as a randomized controlled experimental study with 50 frail patients and their caregivers who underwent knee arthroplasty surgery at the orthopedic ward of Erzincan Mengücek Gazi Training and Research Hospital between October 2025 and June 2026. Patients and caregivers will be assigned to experimental (25) and control (25) groups using a simple randomization method. A mixed design, randomized controlled experimental, and phenomenological study is planned to determine the effects of this study on the feeling of entrapment and caregiver burden of caregivers and on patient satisfaction.

Data collection: The Descriptive Characteristics Form will be applied to the patients' primary caregivers and their relatives. Then, the Feelings of Entrapment Scale, the Zarit Burden of Care Scale, the Caregiver Satisfaction Assessment Index (CASI-TR) and the Patient Satisfaction Assessment Form According to Watson Recovery Processes will be applied to the patients. Then, after the recovery care procedures are completed, on the 4th postoperative day, the Feelings of Entrapment Scale, the Zarit Burden of Care Scale, the Caregiver Satisfaction Assessment Index (CASI-TR) and the Patient Satisfaction Assessment Form According to Watson Recovery Processes will be applied to the patients. Then, the questions in the semi-structured interview form will be asked and their answers will be transferred as is, without any comments. They will also be audio-recorded to prevent data loss and to ensure that the responses can be listened to again by the researcher later. The Feelings of Entrapment Scale, the Zarit Caregiver Burden Scale, and the Caregiver Satisfaction Assessment Index (CASI-TR) will be administered to the primary caregivers and patients in the control group on Day 4. The Patient Satisfaction Assessment Form will be administered to the patients based on Watson Improvement Processes.

Original Value: No studies have been found in the literature that evaluate the theoretical basis of caregiver care for frail patients undergoing knee arthroplasty surgery, their satisfaction with caregiving, the impact of feeling entrapment, or patient satisfaction. In this respect, the project has unique value and will contribute scientifically to national and international literature. If successful, it is expected to introduce holistic nursing care practices to the field regarding the care of frail patients undergoing knee arthroplasty surgery, which presents significant challenges for caregivers. In this respect, the project has unique value.

Expected Outcome: If the project is successful, it will reduce anxiety and caregiver burden in patients' relatives and increase patient-family interaction, contributing to improved patient care and economic efficiency.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Literate
  • Speak and understand Turkish
  • Be over 18 years of age
  • Have a patient they care for undergoing knee arthroplasty
  • Be a caregiver for a frail patient who scores 7 or higher on the Edmonton Frailty Scale
  • Provide primary care for the patient
  • Voluntarily participate in the study

Exclusion criteria

Patient-related exclusion criteria:

  • Developing serious surgical complications (e.g., infection, embolism, prosthesis rejection, etc.) after knee arthroplasty
  • Admission to the intensive care unit after surgery
  • Re-surgery during the postoperative period
  • Death of the patient during the study
  • Voluntary withdrawal from the study or lack of communication

Caregiver-related exclusion criteria:

  • Transfer of caregiving role to another person after the study begins
  • Caregivers experiencing a physical or psychological health problem that would prevent them from continuing the study
  • Caregivers refusing to continue the study or lack of communication

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

50 participants in 2 patient groups

Experimental group
Experimental group
Description:
The study group will consist of patients over the age of 18 who underwent knee arthroplasty surgery at the Orthopedics and Traumatology Clinic of Erzincan Binali Yıldırım University Mengücek Gazi Training and Research Hospital, who have been hospitalized for at least four days postoperatively, and who have a score of ≥7 on the Edmonton Frailty Scale, as well as caregivers over the age of 18 who are the primary caregivers of these patients (both groups must meet criteria such as proficiency in Turkish and volunteering for the study). A total of 25 patients and 25 caregivers will participate in the experimental group.
Treatment:
Behavioral: nursing care
Control group
No Intervention group
Description:
The study group will consist of patients over the age of 18 who underwent knee arthroplasty surgery at the Orthopedics and Traumatology Clinic of Erzincan Binali Yıldırım University Mengücek Gazi Training and Research Hospital, who have been hospitalized for at least four days postoperatively, and who have a score of ≥7 on the Edmonton Frailty Scale, as well as caregivers over the age of 18 who are the primary caregivers of these patients (both groups will meet criteria such as proficiency in Turkish and volunteering for the study). A total of 25 patients and 25 caregivers will participate in the control group.

Trial contacts and locations

1

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Central trial contact

Ilknaz K KARA

Data sourced from clinicaltrials.gov

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