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The validity and reliability of the University of California,Los Angeles (UCLA) shoulder score for use as a self assessment postal questionnaire in patients following rotator cuff surgery to assess outcome

The validity and reliability of the University of California, Los Angeles (UCLA) shoulder score for use as a self assessment postal questionnaire in post rotator cuff surgery assessment.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12606000194561
Acronym
UCLA'
Enrollment
100
Registered
2006-05-24
Start date
2004-07-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The UCLA shoulder score is used to asess the outcome of rotator cuff surgery in the shoulder. Currently this score is assessed clinically- requiring patients to attend for a doctor's appointment. The hypothesis is that with adequate instruction the patient could complete this form at home and this would increase participation in studies which may follow up patients 10 years later. These patients would not have to travel long distances for a clinical assessment for research purposes only. Patients, assessors 1 & 2 are blinded.

Interventions

The UCLA questionnaire is completed by the patient at home within 24 hours of attending for a post operative appointment and handed in a sealed opaque envelope to a receptionist and stored unopened until data entry. This takes the patient 5-10 minutes. Separately and in computer generated random order the patient is physically assessed by 2 outcome assessors in separate rooms and separate UCLA forms are completed by each assessor , sealed in opaque envelopes and stored separately until data entr

The UCLA questionnaire is completed by the patient at home within 24 hours of attending for a post operative appointment and handed in a sealed opaque envelope to a receptionist and stored unopened until data entry. This takes the patient 5-10 minutes. Separately and in computer generated random order the patient is physically assessed by 2 outcome assessors in separate rooms and separate UCLA forms are completed by each assessor , sealed in opaque envelopes and stored separately until data entry is commenced. These forms are completed at 2 months following subacromial decompression and 4 months following rotator cuff repair.

Sponsors

Simon Bell
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Informed consent.Assessment at 2 months after subacromial decompression.At 4 months after rotator cuff repair.

Exclusion criteria

Not having had rotator cuff surgery.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026