Enhanced Rehabilitation After Major Trauma (PROPERLY)

The goal of this study is to assess the feasibility of recruitment, and barriers to delivery of an enhanced rehabilitation service, in patients surviving major trauma.The main questions it aims to answer are:are the investigators able to recruit patients to a research study are the investigators able to retain patients in the research study are the investigators able to identify appropriate primary outcome measures are the investigators able to identify barriers to future large-scale definitive trial or service delivery Participants will would be offered at least two sessions of the Enhanced Rehabilitation Programme (ERP), each lasting 60-120 minutes per week, delivered in the Manchester Institute of Health and Performance (MIHP).Participants not willing to travel to the MIHP, or declining to engage in the ERP, will be asked to join the Standard Care (SC) group. This group will provide questionnaire data and clinical outcome measure collection with their usual place of therapy.Researchers will compare the ERP group and the SC groups to assess any additional benefits to the ERP.

Inclusion Criteria:Participants over 18 years oldRegistered GP in Greater Manchester or Greater Manchester Resident.Polytrauma or one or more complex /severe isolated injuryRehabilitation goals (e.g., mobility, function, job retention/ return to work) identified using shared decision-making processPatient able to enter programme 6-30 months post injury.For the ERP patients willing to travel to the MIHP for their evaluation and treatment twice a week.Participants with lower limb injuries that continue to have functional impairment.Participants deemed well and safe enough to participate by clinical teams.Normal ECG if previously reported to have abnormal ECGParticipants willing to consent to follow up over 12 monthsParticipants with the capacity to consent to the study.Fully healed wounds and bone healed sufficiently to allow at least partial weight bearingExclusion Criteria:Participants under the age of 18Participants unable to provide informed consentParticipants with multiple pre-existing comorbidities that affect ability to participate in enhanced rehabilitation such as cognitive impairment, unstable angina.Central motor neurological impairment affecting ability to participate in an enhanced rehab programmeAbsence of functional disability affecting gait and / or function.Plans for further surgery that will impact on gait or function.