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Trial registered on ANZCTR
Registration number
ACTRN12614001007628
Ethics application status
Approved
Date submitted
10/09/2014
Date registered
18/09/2014
Date last updated
24/07/2020
Date data sharing statement initially provided
24/07/2020
Type of registration
Prospectively registered
Titles & IDs
Public title
Hip arthroscopy effect on physical activity and pain
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Scientific title
In patients with a symptomatic hip labral tear, does hip arthroscopy improve physical activity level, pain and quality of life?
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Secondary ID [1]
285317
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Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Hip labral tear
293032
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Condition category
Condition code
Musculoskeletal
293302
293302
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0
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Arthroscopic hip surgery entails inserting a small camera into the hip joint to enable the surgeon to view, diagnose and treat hip pathology of the labrum, articular cartilage, or other soft tissues surrounding the joint. The surgeon inserts other instruments through separate incisions to smooth off or repair torn cartilage, trim bone spurs and/or remove inflamed synovial tissue. The procedure takes 30-45 minutes.
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Intervention code [1]
290229
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Treatment: Surgery
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Comparator / control treatment
Preoperative compared to 3 month and 1 year postoperative status
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
293140
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Average daily steps taken assessed using a wearable accelerometer
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Assessment method [1]
293140
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Timepoint [1]
293140
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Preoperative, 3 months, 1 year
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Primary outcome [2]
293141
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Pain report using a 100mm visual analogue scale anchored with 2 descriptors "no pain at all" and "extreme pain"
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Assessment method [2]
293141
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Timepoint [2]
293141
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Preoperative, 3 month, 1 year
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Secondary outcome [1]
310437
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Quality of Life iHOT-12 survey
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Assessment method [1]
310437
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Timepoint [1]
310437
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Preoperative, 3 months, 1 year
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Secondary outcome [2]
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Satisfaction level assessed using a 5 point likert scale (very satisfied, satisfied, neutral, dissatisfied, very dissatisfied)
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Assessment method [2]
310438
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Timepoint [2]
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3 months and 1 year postoperative
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Eligibility
Key inclusion criteria
- Patients with acetabular labrum pathology who are candidates for arthroscopic hip surgery as determined by the surgeon and patient.
- Patients who understand the conditions of the study and are willing to participate with follow up
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Minimum age
18
Years
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Maximum age
60
Years
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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
- Previous major ipsilateral hip surgery.
- Evidence of boney hip pathology other than femoroacetabular impingement (e.g. fracture, avascular necrosis, osteomyelitis, osseous neoplasm).
- Women who are pregnant or seeking to become pregnant during the study period.
- Patients who are a prisoner, currently being treated for a psychiatric disorder, senile dementia, Alzheimers disease, or known alcohol abuse
- Patients with comorbidities rendering them house-bound with severe mobility impairment (e.g. Limb amputation, Multiple Sclerosis, Muscular DystrophyParkinson’s Disease, cerebrovascular accident, lower limb fracture, severe back pain).
- Patients with known metal allergy.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Prospective, single-centre, non-randomised, clinical study. The study will enrol 50 participants over a 12 month period
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
3/11/2014
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Actual
9/02/2015
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Date of last participant enrolment
Anticipated
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Actual
29/06/2016
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Date of last data collection
Anticipated
29/06/2017
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Actual
29/06/2017
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Sample size
Target
50
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Accrual to date
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Final
40
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
2975
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Hollywood Private Hospital - Nedlands
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Recruitment postcode(s) [1]
8686
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6009 - Broadway Nedlands
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Funding & Sponsors
Funding source category [1]
289940
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Other
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Name [1]
289940
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The Joint Studio Research Fund
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Address [1]
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1/ 86 Monash Ave
Nedlands WA 6019
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Country [1]
289940
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Australia
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Primary sponsor type
Other
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Name
The Joint Studio
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Address
1/ 86 Monash Ave
Nedlands WA 6019
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Country
Australia
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Secondary sponsor category [1]
288629
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None
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Name [1]
288629
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Address [1]
288629
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Country [1]
288629
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
291654
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Hollywood Private Hospital Ethics
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Ethics committee address [1]
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Monash Ave, Nedlands, WA 6009
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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08/09/2014
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Approval date [1]
291654
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18/12/2014
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Ethics approval number [1]
291654
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HPH390
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Summary
Brief summary
Taking 10,000 steps a day is promoted by The Centres of Disease Control and Prevention, and The American College of Sports Medicine to equate to a healthy level of physical activity (Pate et al, 1995). Through the use of wearable activity monitors, this study will objectively quantify the limitation in physical activity that hip labral tear patients subjectively report. The study aims to determine whether hip arthroscopic surgery improves physical activity, pain, and quality of life. Satisfaction with surgery will also be assessed and provide further insight into the efficacy of arthroscopic hip surgery.
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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
51358
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Dr Dan Fick
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Address
51358
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The Joint Studio
Suite 1, Hollywood Medical Centre
86 Monash Ave
Nedlands WA 6009
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Country
51358
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Australia
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Phone
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+61 8 93863933
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Fax
51358
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Email
51358
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[email protected]
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Contact person for public queries
Name
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Samantha Haebich
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Address
51359
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The Joint Studio
Suite 1, Hollywood Medical Centre
86 Monash Ave
Nedlands WA 6009
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Country
51359
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Australia
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Phone
51359
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+61 8 93863933
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Fax
51359
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Email
51359
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[email protected]
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Contact person for scientific queries
Name
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Samantha Haebich
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Address
51360
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The Joint Studio
Suite 1, Hollywood Medical Centre
86 Monash Ave
Nedlands WA 6009
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Country
51360
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Australia
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Phone
51360
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+61 8 93863933
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Fax
51360
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Email
51360
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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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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