To Investigate the Effect of Early Community-care Program on Fracture Hip Patient

NCT ID: NCT01537523

Last Updated: 2012-02-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-02-29

Study Completion Date

2014-04-30

Brief Summary

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The early community-care program is well-known rehabiliation for the fracture hip patient. For the discharged fracture hip patient from hospital, it is worth to investigate the effect of early mobilization program to improve their physical and psychological aspects.

Detailed Description

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60 fractured hip patient will randomized allocated into intervention group and control group.

The community-care include nursing care, physiotherapy and home modification according to the condition of the patient.

The intervention will received community-care program for 12 weeks. Two sessions per week and total 24 sessions.

The control group will receive the traditional medication. The outcome measure include elderly mobility scale and happiness scale. The measurement will take at initial and completion of the program.

SPSS will be used for data analysis.

Conditions

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Fracture

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Investigators

Study Groups

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community-care program

receive intervention for 12 weeks

Group Type EXPERIMENTAL

community-care program

Intervention Type PROCEDURE

community nurse care, physiotherapy

control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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community-care program

community nurse care, physiotherapy

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* fracture hip patients discharged from queen mary hospital

Exclusion Criteria

* cognitive impairment
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hong Kong Healthcare Volunteer Organization

OTHER

Sponsor Role lead

Responsible Party

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MR L

Chief Executive Officer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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HO HO, MSc

Role: STUDY_DIRECTOR

Volunteer department

Central Contacts

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Man PM Fung, FHKCP

Role: CONTACT

852-24435671

Other Identifiers

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RCT-001

Identifier Type: -

Identifier Source: org_study_id

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