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Feasibility of TRAK to support physio in anterior cruciate ligament rehabilitation

Testing the feasibility of TRAK, an eHealth intervention to support physiotherapy rehabilitation for patients following anterior cruciate ligament reconstructive surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN55635910
Enrollment
50
Registered
2019-07-24
Start date
2018-07-16
Completion date
Unknown
Last updated
2023-08-28

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

Conditions

Rupture of the anterior cruciate ligament Musculoskeletal Diseases

Interventions

This study will use convergent parallel mixed methods where both qualitative and quantitative types are important for thorough understanding of the objectives and where qualitative data may help to in
usual care and usual care plus TRAK. Both groups will receive the usual care for their hospital trust. The TRAK group will be able to monitor the exercises on the website, log their progress and rece

Sponsors

Homerton University Hospital NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adults immediately post ACL reconstruction 2. Referred to a structured NHS rehabilitation programme 3. Be able to read and write English to engage with learning materials on TRAK 4. Be able to give written informed consent themselves 5. Have access to the internet at home or on their phone

Exclusion criteria

Exclusion criteria: 1. Individuals with complex co-morbidities or surgeries such as multi-ligament reconstruction or fracture 2. Lack of internet or smart phone access 3. Unable to read and write English

Design outcomes

Primary

MeasureTime frame
1. Recruitment measured by number of eligible patients who consent to participate from 16/07/2018 until 31/03/2019, and submitted to baseline measures and randomisation 2. Retention measured by number of patients still in trial and consenting to outcomes at 3 and 6 months after recruitment date 3. Feasibility of collecting outcomes measured by collecting outcomes relevant for a future trial at baseline, 3 and 6 months 4. Feasibility of collecting strength outcome measured by submitting patient to leg symmetry testing at 3 and 6 months

Secondary

MeasureTime frame
1. Usage of the intervention is measured by number of logins, number of pages visited and number of videos watched at 3 and 6 months 2. Knee function measured by KOOS (knee injury & osteoarthritis outcome score) at baseline, 3 months and 6 months 3. Health resource use measured by CSRI at baseline, 3 and 6 months 4. Self-efficacy measured by Stanford self-efficacy questionnaire at baseline, 3 and 6 months 5. Quality of life years calculated by EQ5D5L measured at baseline, 3 and 6 months 6. Health economic data collected by WPAI (work productivity and activity impairment questionnaire: general health) measured at baseline, 3 and 6 months

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026