- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00735033
The Effects of the Swiss Ball on Cerebral Vascular Accident
August 18, 2008 updated by: Fortaleza University
The Effects of the Swiss Ball on Patients With Hemiplegia Due to Cerebral Vascular Accident
The objective of this study was to investigate the effects of the Swiss ball on patients with hemiplegia due to CVA.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The Cerebral Vascular Accident (CVA) is a neurological deficit, which may be transitory or definite, leading to motor, psychological and social alterations.
It's the third cause of death in the industrialized world, of which 90% of the survivors have some residual deficit and 30% become disabled.
The objective of this study was to investigate the effects of the Swiss ball on patients with hemiplegia due to CVA.
An intervening and controlled study was conducted on 12 patients of both genders and over 50 years old with chronic hemiplegia, all undergoing treatment at the Beneficent Rehabilitation Association of Ceará.
The patients in the experimental group (EG) underwent treatment with the Swiss ball added to conventional physical therapy and the control group (CG) went through conventional physiotherapy sessions.
The treatment was done twice a week, consisting of 14 sessions altogether.
The data were collected in an evaluation form at the beginning and at the end of the treatment.
Most patients were found to be males; they had typical walking ability, tonus, and posture of chronic hemiplegia patients.
The patients in the experimental group showed significantly greater muscular strength on the lower limbs than the control group (p < 0,05, Student t test), however, the same did not happen in the case of the other parameters, such as strength on the upper limbs, coordination, and balance.
We can conclude that the treatment with the Swiss ball can promote increased strength, which will allow for a more efficient recovery in the studied population.
Study Type
Interventional
Phase
- Not Applicable
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
19 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Hemiplegia due to CVA
- In physiotherapy treatment
- Acceptance in join the research
Exclusion Criteria:
- Less then 6 months of diagnostic
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: Treatment
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 Registration Dates
First Submitted
August 12, 2008
First Submitted That Met QC Criteria
August 13, 2008
First Posted (Estimate)
August 14, 2008
Study Record Updates
Last Update Posted (Estimate)
August 19, 2008
Last Update Submitted That Met QC Criteria
August 18, 2008
Last Verified
May 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- coetica-130/2004
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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