HIP Fracture REhabilitation Programme

Hip Fractures Clinical Trial

— HIP-REP  

Official title:

HIp Fracture REhabilitation Programme for Elderly With Hip Fracture

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04207788
• Other study ID #: H-19066989
• Status: Completed
• Phase: N/A
• Start date: January 28, 2020
• Est. completion date: April 30, 2021

Study information

• Verified date: March 2022
• Source: Herlev and Gentofte Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Objectives: To evaluate the effect of a HIP-REP on the quality and independence in ADL ability (performance), measured with the Assessment of Motor and Process Skills (AMPS) and health-related Quality of Life (QoL). Hypothesis: The HIP-REP will increase the quality and independence in ADL performance, measured with AMPS and health-related QoL measure.

Description:

Little is known about the effect of an intersectoral rehabilitation intervention aiming at reducing the decrease in Activities of Daily Living (ADL) ability for elderly with hip fractures. Despite positive surgical outcomes, one-quarter dies within a year after surgery, around eight percent are readmitted to hospital, and just one-third regain their pre-fracture level of physical functioning and ADL ability. After hip fracture, the loss of independence, and further decrease in ADL ability often persists beyond three months after surgery. This increases the risk of social isolation, depression and thus a decrease in QoL. Therefore, the investigators want to evaluate whether an activity-based rehabilitation intervention across sectors is effective and influences this fragile group of patients. The investigators hope to increase the ability to safely and independently perform ADL in elderly with hip fractures, and thereby enhance their health-related QoL.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: April 30, 2021
• Est. primary completion date: March 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 65 Years and older

Eligibility

Inclusion Criteria:

• Aged 65 years or older
• Recent proximal hip fracture (S 72.0 medial femur fracture, S 72.1, pertrochanteric femur fracture, S 72.2 subtrochanteric femur fracture)
• Living at home prior to hip fracture in Herlev, Gentofte, Furesoe, Rudersdal or Lyngby-Taarbæk municipalities
• Ability to give informed consent

Exclusion Criteria:

• Not expected to be discharged to home or rehabilitation centers in the municipality
• Not able to speak and/or understand Danish
• Have prior severe physical and /or mental disabilities

Related Conditions & MeSH terms

• Fractures, Bone
• Hip Fractures

Intervention

Other:
• HIP-REP
HIP-REP programme is an add on to usual care which includes 5 add on individual activity-focused interventions that will be tailored to the need of elderly with hip fracture in a liaison with the health care professionals. Home visits and follow-up phone call will be a part of programme.
• Usual care
The elderly in the control group will receive usual rehabilitation. with a focus on mobilization within 24 hours postoperative as an in-patient. In the municipality physiotherapy is offered twice a week for approximately 12 weeks postoperative focusing on neuromotor control over hip, activation and strengthening of muscles as well as increase mobility. When relevant, the elderly receives a home visit by an occupational therapist who assess ADL behaviours, the use of assistive devices and the environmental hazards, preparing and adapting the home environment to prevent falls.

Locations

Country	Name	City	State
Denmark	Department of Physiotherapy and Occupational Therapy, Copenhagen University Hospital, Herlev and Gentofte	Copenhagen	Herlev

Sponsors (12)

Lead Sponsor	Collaborator
Carsten Bogh Juhl	Danish Association of Occupational Therapist, Danish Regions Development and Research, Herlev and Gentofte Hospital, Intersectoral Research Unit, Jonkoping University, Metropolitan University College, Municipality of Furesoe, Municipality of Gentofte, Municipality of Herlev, Municipality of Lyngby-Taarbaek, Municipality of Rudersdal

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment of Motor and Process Skills	The assessment measures the quality of a person's activity of daily living task performance. An observational assessment that allows for evaluation of change in motor and process skills and their effect on the ability of an individual to perform complex or instrumental and personal activities of daily living. The instrument consists of 16 motor and 20 process skill abilities that are rated on a 4-point scale. The rating scale is based on the following criteria (Quality of performance); 4 = Competent, 3 = Questionable, 2 = Ineffective or 1 = Severely deficient. In all, 36 discrete ratings of motor and process skills are made during observation.	Change frombaseline at motor and process skills 3 and 6 months after baseline testing
Secondary	European Quality of Life Questionnaire	A survey collecting information about health related quality of life comprising five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems.	At baseline and 3 and 6 months after baseline testing
Secondary	Verbal Rating Scale	An assessment measuring the intensity of pain. The patient chooses one of those: none, mild, moderate or severe.	At baseline and 3 and 6 months after baseline testing
Secondary	Functional Recovery Score	Functional Recovery Score assess the level of function with eleven-items comprised of three main components: basic activities of daily living assessed by four items, instrumental activities of daily living assessed by six items, and mobility assessed by one item. Basic activities of daily living comprise 44 percent of the score; instrumental activities of daily living comprise 23 percent, and mobility comprises 33 percent. Complete independence in basic and instrumental activities of daily living and mobility results in a score of 100percent.	at baseline and 3 and 6 months after baseline testing