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Occupational advice for patients undergoing arthroplasty of the lower limb

Not Applicable
Completed
Conditions
Specialty: Musculoskeletal disorders, Primary sub-specialty: Other
UKCRC code/ Disease: Musculoskeletal/ Other disorders of the musculoskeletal system and connective tissue
Musculoskeletal Diseases
Arthritis
Registration Number
ISRCTN27426982
Lead Sponsor
South Tees Hospitals NHS Foundation Trust
Brief Summary

2018 protocol in: https://www.ncbi.nlm.nih.gov/pubmed/29950166 2020 delphi study results in https://pubmed.ncbi.nlm.nih.gov/32636283/ (added 09/07/2020) 2020 results in https://pubmed.ncbi.nlm.nih.gov/32930659/ (added 16/09/2020)

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
310
Inclusion Criteria

Phase 1:
1. Age 16 years and above
2. Patients undergoing primary hip or knee replacement
3. In work within 6 months prior to joint replacement (including Full time, Part time, Paid & unpaid job roles)

Phase 2
1. Inclusion criteria as listed for Phase 1
2. Patients intending to return to work following surgery

Stakeholder interviews/focus groups (phase 1 & 2) or Delphi consensus process (phase 2) will include some patients (as above), AHP, GPs, Orthopaedic surgeons and Employer representatives. Orthopaedic surgeons, AHPs , GPs and employers would have to be involved directly in the care of patients undergoing hip and knee replacement procedures in the preceding 12 months. Orthopaedic consultants undertaking a minimum of 20 Total Hip or Knee Replacement operations per year will be eligible as this threshold will encompass surgeons with a specific interest in hip and knee replacements that are more likely to have experience of patients that return to work following surgery. AHPs involved in the current care pathways at each centre will be recruited. GPs with experience of treating patients undergoing either hip and knee replacements in the previous twelve months will be eligible.

Exclusion Criteria

Phase 1 & 2:
1. Lack of mental capacity to understand and participate in the cohort study
2. Patients who do not understand written and spoken English
3. Emergency surgical procedure e.g. Surgery for an indication of trauma
4. Surgery for cancer
5. Surgery for infection

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Return to work rate is assessed at 16 weeks
Secondary Outcome Measures
NameTimeMethod
<br> Following outcomes are measured at baseline, 8 and 16 weeks. Also measured at 24 weeks for first 45 patients.<br> 1. Functional status:<br> 1.1. Joint function, measured using the Oxford hip / knee score<br> 1.2. Health utility, measured using the EQ5D-5L<br> 1.3. Workplace disability and participation, measured using the Workplace limitations Questionnaire (WLQ), Elements of the Workplace design questionnaire (WDQ), PHQ - 9 (Patient health questionnaire), Brief resilience scale (BRS) and GAD-2 (Generalised anxiety disorder scale - 2)<br> 2. Occupational information<br> 3. Use of fit notes<br> 4. Healthcare utilisation and adherence with rehabilitation programmes<br> 5. Details of interactions with occupational health practitioners / departments<br> 6. Details of occupational advice received<br> 7. Return to driving following surgery<br>
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