Motivational Interview for Daily Living Activities in Elderly People Undergoing Total Knee Replacement (Motivation)

December 28, 2022 updated by: Gizem KUBAT BAKIR, Maltepe University

The Effect of Motivational Interview for Daily Living Activities on Physical Adjustment and Quality of Life in Elderly People Who Have Had Total Knee Replacement

Purpose: In this study, it was aimed to examine the effect of motivational interview on daily living activities on physical adaptation and quality of life in elderly people who underwent total knee replacement.it was aimed to examine the effect of motivational interview on daily living activities on physical adaptation and quality of life in elderly people who underwent total knee replacement.

Design: The research was planned as a pretest, posttest, randomized controlled study in order to determine the effect of the motivational interviews on the life quality and physical activity of old patients.

H1: After total knee replacement, the target for daily living activities is higher than the patients who applied the hand and those who did not.

H2: Patients with targeted daily living activities with total knee replacement begin to get used to it and begin earlier than those who do not.

Study Overview

Study Type

Interventional

Enrollment (Actual)

70

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • İ̇stanbul
      • Ataşehi̇r, İ̇stanbul, Turkey
        • Gizem Kubat Bakir

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years to 90 years (Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Those aged 65 and over,
  • Having total knee replacement,
  • The non-spiritual system (the peasant of the sick),
  • A person who can read and write can cope at a level that prevents conversation,
  • First time system add-on,
  • They are viewed as agreeing to participate in the research.

Exclusion Criteria:

  • Neurological (such as dementia) and psychiatric (such as schizophrenia) medical diagnoses that affect cognitive status
  • Patients who did not participate in the motivational interviews and who wanted to leave the study were determined.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Motivational interview
8 motivational interviews were conducted with the intervention group.
The motivational interviewing technique is a client-focused, directive form of counseling to create behavior change. Its main goal is to discover and solve ambivalence. This method is especially useful for people who are reluctant or ambivalent to change.
Active Comparator: Control Group
No application was made to increase physical compliance and improve quality of life.
Patients with total knee replacement receive standard nurse care. Treatment is applied. He does his own exercises at home.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The SF-36 Quality of Life Scale
Time Frame: For 3 months
The SF-36 Quality of Life Scale consists of 8 subgroups and 36 questions. The fourth and fifth questions of the SF-36 scale are yes/no, the other questions are likert type (3, 5 and 6). Items 1, 6, 7, 8, 9a, 9d, 9e, 9h, 11b, 11d in the scale are calculated by reversing them. The physical and mental summary value of the scale is obtained by adding the weighted scores of the questions containing the sub-scales of the SF-36 quality of life scale. There is no total score. The scores obtained range from zero to one hundred. Zero indicates poor health and 100 indicates good health.
For 3 months
Functional Evaluation Form
Time Frame: For3 months
The Functional Evaluation Form consists of 8 sections, including maximum walking distance, use of walking aids, getting up from a chair, climbing stairs, working status, daily tasks, transportation and lower extremity care, and each section is self-contained (first four sections are out of 15 points, the remaining four sections are out of 10 points). The highest total score is 100. An increase in the score indicates functional improvement.
For3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: GİZEM KUBAT BAKIR, Gizem Kubat Bakir

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 2, 2020

Primary Completion (Actual)

May 25, 2021

Study Completion (Actual)

July 26, 2021

Study Registration Dates

First Submitted

September 13, 2021

First Submitted That Met QC Criteria

October 19, 2021

First Posted (Actual)

October 29, 2021

Study Record Updates

Last Update Posted (Estimate)

December 29, 2022

Last Update Submitted That Met QC Criteria

December 28, 2022

Last Verified

December 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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