Evaluation of an Intervention Program Targeted at Improving Balance and Functional Skills After Stroke
NCT ID: NCT00377689
Last Updated: 2008-10-29
Study Results
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.
COMPLETED
PHASE2
34 participants
INTERVENTIONAL
2006-09-30
2008-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
High intensity exercise have shown to be effective for improving strength and balance for older people in general living in residential care facilities. It is interesting to see if this high intensity exercise also is applicable in the older stroke population.
Comparison: An intervention group receives three training sessions per week and one theory session per week during 5 weeks, compared to a control group that receives one theory session per week during 5 weeks.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
DOUBLE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
high intensity functional exercise
high intensity functional exercise
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* stroke diagnosis 3-6 months prior to inclusion
* ability to walk 10 meter with or without assistive device
* ability to understand simple instructions
Exclusion Criteria
* independent in walking outdoors
* serious visual impairment
* serious hearing impairment
* long distance to intervention station
55 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Vardalinstitutet The Swedish Institute for Health Sciences
OTHER
Erik & AnnMarie Detlofs Foundation
UNKNOWN
The Swedish National Stroke society
UNKNOWN
The Northern County Councils Regional Federation
UNKNOWN
Umeå University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Umea University
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Eva Holmgren, PhD student
Role: PRINCIPAL_INVESTIGATOR
Umeå University & The Vårdal Institute
Per Wester, MD Professor
Role: STUDY_CHAIR
Umeå University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Umeå University, department of Community science and rehabilitation
Umeå, , Sweden
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Dnr 04-022
Identifier Type: -
Identifier Source: org_study_id