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Using a shared decision-making tool with adults after an anterior cruciate ligament injury

The PreOperative management of Patients awaiting Anterior Cruciate Ligament Reconstruction (POP-ACLR) feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17801081
Enrollment
20
Registered
2024-01-23
Start date
2024-01-29
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Anterior cruciate ligament reconstruction Musculoskeletal Diseases

Interventions

Recruitment and procedure Potential participants will be identified by the orthopaedic team during the patients clinical appointment where they are diagnosed with an ACL rupture. The recruitment of pa

Sponsors

University Hospitals of Derby and Burton NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Feasibility: 1. >=18 years old 2. Confirmed first-time ACL rupture via MRI Qualitative interviews: 1. Clinician or patient with experience of using the SDM tool

Exclusion criteria

Exclusion criteria: Feasibility: 1. Concomitant injuries requiring surgical intervention that will significantly alter usual treatment e.g. fracture 2. Previous knee surgery to the affected limb 3. Pregnancy (as this is likely to affect decision-making regarding surgical treatment)

Design outcomes

Primary

MeasureTime frame
Four feasibility outcomes measured at the end of the study: 1. Recruitment rate measured as the number of eligible participants who consent to participate in the study 2. Fidelity measured by reviewing the case report form to establish the content of the clinical consultation against the predefined SDM tool content/guidance delivered during training to physiotherapists 3. Acceptability measured using an acceptability questionnaire completed by participants within 4 weeks of their clinical consultation using the SDM tool 4. Follow-up questionnaire completion measured as the number of questionnaires completed by participants

Secondary

MeasureTime frame
1. Satisfaction with treatment decision will be measured using the satisfaction with decision (SWD) scale up to 4 weeks following the clinical consultation where the SDM tool is used 2. Implementation factors will also be explored through individual qualitative semi-structured interviews conducted with patient participants and treating clinicians after completion of the clinical consultation

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 19, 2026