Effects of a Late Phase Exercise Program Following Total Hip Arthroplasty

NCT ID: NCT00896259

Last Updated: 2012-08-29

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

47 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-03-31

Study Completion Date

2011-02-28

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

A group of orthopedic physiotherapists have developed a late phase program to educate and instruct total hip replacement patients in progressive exercises appropriate for their level of recovery. The components of this program include an educational presentation, individual assessment and exercise prescription. The investigators' intent is to pilot the program using a sample of patients. The objective of this pilot project:

To examine the effects of the late phase education session and home-based exercise program in restoring hip muscle strength, gait and function

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Total Hip Arthroplasty

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Unilateral total hip arthroplasty

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

THA control

those with THA not participating in exercise and education program

No interventions assigned to this group

THA exercise

those with THA and participating in exercise and education program

home based exercise and education program

Intervention Type OTHER

Individual assessment with physiotherapist with educational information, exercise instruction and prescription provided. Instructed to perform home exercises and walking for 12 weeks. Will be individually tailored to participants, bi-monthly phone calls will be used to monitor and facilitate exercise and walking progression .

healthy control

Healthy control, people with no lower limb gait abnormalities

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

home based exercise and education program

Individual assessment with physiotherapist with educational information, exercise instruction and prescription provided. Instructed to perform home exercises and walking for 12 weeks. Will be individually tailored to participants, bi-monthly phone calls will be used to monitor and facilitate exercise and walking progression .

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* unilateral primary total hip arthroplasty (THA)
* 8-12 weeks post THA
* over the age of 18
* able to walk 15m without a walking aid
* able to participate in an exercise program without physical assistance
* available for follow up as per the study protocol
* able to read and understand English and follow verbal and visual instructions

Exclusion Criteria

* medically unstable
* have central or peripheral nervous system deficits
* have an underlying terminal disease (cancer)
* have suspicion of infection following joint replacement
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Canadian Orthopaedic Foundation

OTHER

Sponsor Role collaborator

Nova Scotia Health Authority

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Kim Parker

Rehabilitation Engineer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Ann Read, BScPT, MSc

Role: PRINCIPAL_INVESTIGATOR

CDHA

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Orthopedic Clinic, QEII Health Sciences Centre, CDHA

Halifax, Nova Scotia, Canada

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Canada

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CDHA-RS/2007-057

Identifier Type: -

Identifier Source: org_study_id