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Trial registered on ANZCTR
Registration number
ACTRN12618000334202
Ethics application status
Approved
Date submitted
23/02/2018
Date registered
6/03/2018
Date last updated
6/03/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Are falls associated with psychological issues in patients undergoing orthopaedic total knee or hip replacement surgery?
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Scientific title
Are falls and falls risk associated with pain catastrophising, anxiety and depression in patients undergoing orthopaedic total knee or hip replacement surgery?
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Secondary ID [1]
294140
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
NIl
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Health condition
Health condition(s) or problem(s) studied:
osteoarthritis
306765
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knee replacement
306766
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hip replacement
306767
0
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falls
306768
0
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anxiety
306769
0
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depression
306797
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Condition category
Condition code
Mental Health
305863
305863
0
0
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Anxiety
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Surgery
305903
305903
0
0
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Other surgery
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
The aim of the study is to determine whether falls, pain catastrophising, anxiety and depression are associated with poorer post-operative outcomes including falls risk, We will be studying the number of falls, physical function, functional mobility, length of stay, and the need for extra rehabilitation services in patients undergoing total knee and hip joint replacement.
Key research questions are:
Does falls risk, anxiety and depression preoperatively predict post operative
poor outcomes following total knee and hip replacement surgery?
Do psychological and physical components have an association in the prediction of falls in the preoperative and post operative periods in the patients having total knee and hip joint replacement?
Method:
Patients will be assessed preoperatively and fill out questionnaires that relate to function, mental well being and also participate in a physical assessment test that includes a physiological profile score for falls and timed up and go tests.
When patients are admitted for the surgery, any falls in the hospital is recorded, length of hospital stay and discharge destination and additional services requirements on discharge also noted.
At 6 weeks post operatively all the questionnaires and the physical assessment are repeated.
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Intervention code [1]
300432
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Diagnosis / Prognosis
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
304942
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falls
Measured from hospital records and also patient reported.
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Assessment method [1]
304942
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Timepoint [1]
304942
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preoperatively at 4-6 weeks when they attend preadmission clinic( primary start point)
at the time of admission and on discharge from the hospital
6 weeks post operatively( primary end point)
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Primary outcome [2]
304943
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anxiety and depression
Questionnaires used (Hospital Anxiety and Depression Scale)
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Assessment method [2]
304943
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Timepoint [2]
304943
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preoperatively 4-6 weeks prior to the surgery
6 weeks post operatively
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Primary outcome [3]
304944
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pain catastrophising
PCS ( pain catastrophising score ) questionnaire used
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Assessment method [3]
304944
0
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Timepoint [3]
304944
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preoperatively 4-6 weeks prior to the surgery
6wks post operatively
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Secondary outcome [1]
343583
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length of hospital stay
Using Hospital records
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Assessment method [1]
343583
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Timepoint [1]
343583
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on admission for surgery and discharge from surgery
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Eligibility
Key inclusion criteria
patients who are having total knee replacement or total hip replacement surgery
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Minimum age
20
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
patients unable to fill forms in English
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Study design
Purpose
Screening
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
Statistical analysis
Descriptive statistics will be used to describe the population study. To compare the characteristics of the sample before and after surgery a range of tests will be performed according to the distribution of the variable of interest. This will include chi-square for categorical variables, parametric tests for normally distributed continuous variables (e.g. t-tests, paired t-tests) and non-parametric tests for non-normally distributed continuous variables (e.g. Mann-whitney tests, and Wilcoxon rank sign tests). Univariate and multiple regression analysis will be used to analyse associations between falls risk and other physiological measures with psychological characteristics (predictors). Significance will be set at p<0.05.
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
12/03/2018
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
200
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
10120
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Concord Repatriation Hospital - Concord
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Recruitment postcode(s) [1]
21654
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2139 - Concord
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Funding & Sponsors
Funding source category [1]
298776
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Hospital
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Name [1]
298776
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Concord Repatriation Hospital
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Address [1]
298776
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Hospital Road
Concord 2139
NSW
Australia
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Country [1]
298776
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Australia
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Primary sponsor type
Hospital
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Name
Concord Repatriation Hospital
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Address
Hospital Rd
Concord2139
NSW
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Country
Australia
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Secondary sponsor category [1]
297960
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None
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Name [1]
297960
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Address [1]
297960
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Country [1]
297960
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
299723
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Human Research ethics commitee Concord Repatriation Hospital
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Ethics committee address [1]
299723
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Hospital Road Concord 2139 NSW
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Ethics committee country [1]
299723
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Australia
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Date submitted for ethics approval [1]
299723
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03/05/2017
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Approval date [1]
299723
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08/11/2017
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Ethics approval number [1]
299723
0
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Summary
Brief summary
The aim of the study is to determine whether falls, pain catastrophising, anxiety and depression are associated with poorer post-operative outcomes including falls risk, number of falls, physical function, functional mobility, length of stay, and the need for extra rehabilitation services in patients undergoing total joint replacement. Key research questions are: Does falls risk, anxiety and depression preoperatively predict post operative poor outcomes following joint replacement surgery? Do psychological and physical components have an association in the prediction of falls in the preoperative and post operative periods in the patients having total joint replacement?
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Mrs Sathiyapriya Gnanakumaran
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Address
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Sydney Local Health District
Concord Repatriation Hospital
Hospital Rd
Concord 2139 NSW Australia
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Country
81374
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Australia
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Phone
81374
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+61421546752
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Fax
81374
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Email
81374
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[email protected]
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Contact person for public queries
Name
81375
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Sathiyapriya Gnanakumaran
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Address
81375
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Sydney Local Health District
Concord Repatriation Hospital
Hospital Rd
Concord 2139 NSW Australia
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Country
81375
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Australia
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Phone
81375
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+61421546752
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Fax
81375
0
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Email
81375
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[email protected]
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Contact person for scientific queries
Name
81376
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Sathiyapriya Gnanakumaran
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Address
81376
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Sydney Local Health District
Concord Repatriation Hospital
Hospital Rd
Concord 2139 NSW Australia
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Country
81376
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Australia
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Phone
81376
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+61421546752
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Fax
81376
0
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Email
81376
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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