- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00819936
A Controlled Trial of Effectiveness of a Backward Walking Program in Patients Recovering From Abdominal Aorta Surgery
January 8, 2009 updated by: Medical University of Silesia
A Controlled Trial of Effectiveness of a Backward Walking Program in Patients Recovering From an Abdominal Aorta Surgery
Summary Question: Does backward walking offer additional therapeutic value in patients after aortic aneurysm surgery?
Participants: The study of backward walking as an addictive physiotherapy procedure was conducted in the group of 65 patients who underwent abdominal aorta surgery.
The patients were randomly divided into three subgroups and three various models of physiotherapy were applied.
Control group has only routine physiotherapy since therapeutic group I and II have also walking exercises forward in group I and backward in group II respectively.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
47
Phase
- Phase 4
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
65 years to 75 years (Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Patients with abdominal aortic aneurysm
- Age 65-75 years
- Male sex
- Stable cardiologic status
- Absence of neurological disorders
- Non-symptomatic aneurysm - non-ruptured
- No pain complaints
- No motion system impairments
Exclusion Criteria:
- Patients with neurological disorders
- Unstable coronary heart disease symptomatic aortic aneurysm - dissecans aneurysm
- Having difficulty in locomotion
- Having contradiction for starting physical training during the first or second day after surgery
- Patients with psychiatric disease
- Lack of patient's compliance with physiotherapist; AND
- Other medical contraindications
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 2
Backward walking,
|
physiotherapy with use a backward walking type of physiotherapy
|
|
Active Comparator: 1
Forward walking
|
comparison forward walking vs backward walking in the physiotherapy after after abdominal surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2005
Primary Completion (Actual)
December 1, 2005
Study Completion
December 1, 2006
Study Registration Dates
First Submitted
January 8, 2009
First Submitted That Met QC Criteria
January 8, 2009
First Posted (Estimate)
January 9, 2009
Study Record Updates
Last Update Posted (Estimate)
January 9, 2009
Last Update Submitted That Met QC Criteria
January 8, 2009
Last Verified
January 1, 2009
More Information
Terms related to this study
Other Study ID Numbers
- B.W 2008/A
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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