ACTRN12620000877987
Completed
未知
Post-operative physiotherapy provided by Allied Health Assistants for Patients with Acute Hip Fracture: a feasibility randomised controlled trial
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Peninsula Health
- Enrollment
- 50
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patient participants
- •Eligible participants will be patients who have undergone surgery for management of hip fracture at the participating acute hospital site. Participants must meet the following eligibility criteria:
- •Inpatient at acute hospital participating site
- •Admission diagnosis of hip fracture (S72\.0–S72\.2 according to the International Classification of Diseases 10th revision (ICD\-10\)
- •Walked independently pre\-hip fracture with or without the use of a walking aid
- •Willingness and ability (i.e. medically stable), as determined by initial physiotherapy assessment, to participate in post\-operative physiotherapy
- •Aged 18 years or older
- •Able to provide written, informed consent
- •Able to communicate in conversational English
- •Staff participants:
Exclusion Criteria
- •Patient Participants:
- •Exclusion criteria are:
- •Patients unable to participate in physiotherapy rehabilitation (e.g. patients with a post\-operative lower extremity touch or non\-weight bearing status)
- •Patients who were non\-ambulant OR required assistance of another person to walk pre\-hip fracture
- •Patient not suitable for mobilisation or physiotherapy
- •Impaired cognition (Short Portable Mental Status Questionnaire Score \<8\)
- •If the patient is not appropriate for mobilisation they will not be eligible for participation in the study. However, participants are eligible for inclusion in the study if their medical stability improves on any day during their admission. Mobilisation will be contraindicated if the patient experiences any of the following complications:
- •Severe post\-operative pain that restricts weight bearing
- •Nausea or vomiting with or without antimetic
- •Vitally unstable: postural blood pressure drop, febrile, bradycardia \<40bpm or abnormal heart rhythm
Outcomes
Primary Outcomes
Not specified
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Postoperativ smärtlindring och mobilisering efter per- och postoperativ injektion av ropivakin, ketorolak och adrenalin givet i operationsområdet, infiltrativt och i knäleden, vid enkammarknäplastikoperation (miniknä)Post-operativ smärta efter enkammarknäplastikoperation, s k miniknäEUCTR2005-000685-39-SEniversitetssjukhuset Örebro40