Skip to content

Fracture in the Elderly Multidisciplinary Rehabilitation (phase 2)

Developing a multidisciplinary rehabilitation package following hip fracture

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN22464643
Enrollment
90
Registered
2014-07-21
Start date
2014-06-09
Completion date
Unknown
Last updated
2019-11-11

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

Conditions

Rehabilitation for people aged 65 and over following surgery for fractured neck of femur Musculoskeletal Diseases

Interventions

Participants are randomised to two groups: 1. Intervention group: A rehabilitation intervention consisting of a workbook and goal setting diary to be held and used by the patient coll

Sponsors

Bangor University (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age 65 years or older 2. Recent proximal hip fracture including the following types of fracture: intracapsular, extracapsular (pertrochanteric, intertrochanteric, reverseoblique or subtrochanteric) 3. Surgical repair by replacement arthroplasty or internal fixation within the previous week; recovering as an in-patient on an orthopaedic ward and not yet discharged home or transferred to an in-patient unit 4. Living independently prior to hip fracture, defined as living in their own home 5. Capacity to give informed consent 6. Living and receiving rehabilitation in the participating NHS site area 7. Carers of patient participants will also be recruited where they provide them with face to face support most days in a week including help with activities of daily living and or physical care

Exclusion criteria

Exclusion criteria: 1. Younger adults with hip fracture 2. Non-surgical treatment following hip fracture 3. Living in residential or nursing homes prior to hip fracture 4. Lack of capacity to give informed consent 5. Participants who are not able to understand Welsh or English 6. Participants who do not live and will not receive community rehabilitation in the participating NHS site area

Design outcomes

Primary

MeasureTime frame
Barthel Index measured at baseline and at 3 months

Secondary

MeasureTime frame
1. Abbreviated Mental Test Score (AMTS) 2. Nottingham Extended Activities of Daily Living Scale 3. Hospital Anxiety and Depression Scale (HADS) Measured at baseline and at 3 months. Process outcomes: 1. Visual Analogue Scale (VAS) for hip pain intensity 2. General Self Efficacy Sale 3. Falls Efficacy Scale - International (FES- I) 4. Self-efficacy for exercise scale 5. Visual Analogue Score - Fear of Falling (VAS-FOF) Health economic measures: 1. EuroQol EQ-5D 2. ICEpop CAPability measure for Older people (ICECAP-O) 3. Client Service Receipt Inventory (CSRI) 4. Discrete Choice Experiment Objective Measures of Physical Function: 1. Grip strength 2. Thirty second sit to stand 3. Eight foot get up and go test Fifty foot walk test: Cohort-study outcomes include: number of patients aged over 65 years admitted with a proximal femoral fracture; the number who fulfil the inclusion criteria for the randomised feasibility study; the number of deaths, serious complications such as falls and repeat fractures, serious illness requiring hospital re-admission and discharged to institutional care (including detail such as the type of ward and the type of residential care)

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 17, 2026