HIP Fracture REhabilitation Programme

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.

Conditions

• Hip Fractures

Interventions

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.

OTHER

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.

Sponsors & Collaborators

• Municipality of Herlev

  collaborator UNKNOWN

• Municipality of Gentofte

  collaborator UNKNOWN

• Municipality of Lyngby-Taarbaek

  collaborator UNKNOWN

• Municipality of Furesoe

  collaborator UNKNOWN

• Municipality of Rudersdal

  collaborator UNKNOWN

• Herlev and Gentofte Hospital

  collaborator OTHER

• Jonkoping University

  collaborator OTHER

• Intersectoral Research Unit

  collaborator UNKNOWN

• Metropolitan University College

  collaborator OTHER

• Danish Association of Occupational Therapist

  collaborator OTHER

• Danish Regions Development and Research

  collaborator UNKNOWN

• Carsten Bogh Juhl

  lead OTHER

Study Design

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Model

PARALLEL

Eligibility

Min Age

65 Years

Sex

ALL

Healthy Volunteers

No

Timeline & Regulatory

Start

2020-01-28

Primary Completion

2021-03-01

Completion

2021-04-30

Countries

• Denmark

Study Locations