- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05100524
Motivational Interview for Daily Living Activities in Elderly People Undergoing Total Knee Replacement (Motivation)
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
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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İ̇stanbul
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Ataşehi̇r, İ̇stanbul, Turkey
- Gizem Kubat Bakir
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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 |
|---|---|
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Experimental: Motivational interview
8 motivational interviews were conducted with the intervention group.
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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.
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|
Active Comparator: Control Group
No application was made to increase physical compliance and improve quality of life.
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Patients with total knee replacement receive standard nurse care.
Treatment is applied.
He does his own exercises at home.
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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.
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For 3 months
|
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Functional Evaluation Form
Time Frame: For3 months
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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.
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For3 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: GİZEM KUBAT BAKIR, Gizem Kubat Bakir
Publications and helpful links
Helpful Links
- Motivational interviewing to increase physical activity in long-term cancer survivors: a randomized controlled trial
- Effectiveness of a motivational interviewing intervention on weight loss, physical activity and cardiovascular disease risk factors: a randomised controlled trial with a 12-month post-intervention follow-up
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 0050
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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