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Effect of Preoperative Education Based on Roy Adaptation Model

Not Applicable
Completed
Conditions
Orthopedic Disorder
Interventions
Other: Education booklet
Registration Number
NCT05248529
Lead Sponsor
Istanbul Medipol University Hospital
Brief Summary

This research was conducted as a randomized controlled experiment to determine the effect of the education given by the Physiological Mode of Roy Adaptation Model in patients with hip or knee arthroplasty on physical adaptation and mobility.

Detailed Description

The research was conducted between 01.11.2017 - 01.04.2018 at the Orthopedics and Traumatology Surgery Service of a private University Hospital in Istanbul.

In the study, the number of samples to be taken; the training, the training group control group mobility scale scores between The Observer at least 5% of the study considering that would make a difference, and power 80%, α=0.05 and power analysis adopted by participants for each group were calculated and it was determined that there should be at least 27.

The sample was composed of 78 individuals 41 experimental and 37 control. Patients' physical adaptation and mobility were evaluated using the Patient Mobility Scale and Observer Mobility Scale and Physical Adaptation Assessment Form.

Randomization of the study was achieved by planning patients who met the inclusion and non-inclusion criteria for training and control groups sequentially, without dividing them into hip or knee arthroplasty. In the randomization table, those with the number 1 are assigned to the training group.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
78
Inclusion Criteria

can read and write in Turkish A sufficient level of education to understand study procedures and training

Exclusion Criteria

hospitalized due to fracture mental disability neurological disease undergone the same operation before received similar training before

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupEducation bookletWithin 12-24 hours before the surgery, the demonstrative education was given based on 'Hip Replacement Adaptation Booklet' and 'Knee Replacement Adaptation Booklet' to the patients in the intervention group.
Primary Outcome Measures
NameTimeMethod
Body Mass Index5 days

Body Mass Index is a simple calculation using a person's height and weight. The formula is BMI = kg/m2 where kg is a person's weight in kilograms and m2 is their height in metres squared.

height5 days

height in meters. it was used to determine the body mass index.

Systolic and diastolic blood pressure5 days

Both systolic and diastolic blood pressure is measured in units of millimeters of mercury (mmHg). It was used to determine the blood pressure of patients before mobilization.

Weight5 days

weight in kilograms. It was used to determine the body mass index.

Secondary Outcome Measures
NameTimeMethod
The Patient Mobility Scale5 days

As a scale score, 1 indicates that the patient has no pain during the activity and the level of difficulty when moving is minimal, while 5 indicates that the patient's pain during the activity is unbearable and the level of difficulty is greatest. The lowest score that can be obtained from the scale is 8 and the highest score is 40.

The Observer Mobility Scale5 days

1 point indicates that the activity can be performed independently without verbal warning and physical assistance, 5 points indicate that the patient cannot perform the activity independently despite the verbal warning and physical assistance. The lowest score that can be obtained from the scale is 4 and the highest score is 20.

Trial Locations

Locations (1)

Yeditepe University Hospital

🇹🇷

Istanbul, Turkey

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