Standardized Physical Activities Measured by Accelerometers
NCT ID: NCT01629342
Last Updated: 2012-06-28
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.
UNKNOWN
25 participants
OBSERVATIONAL
2012-06-30
2012-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Methods: Patients discharged since February 2012 after a transient ischemic attack have been invited to participate in the study scheduled for June-September 2012 (nexpected=25). All participants wear 5 accelerometers (Actical), one at each wrist and ankle and one over the hip. Standardized physical activities include:
* treadmill walking (5 minutes, 1 and 4km/h)
* staircase walking (1 floor, normal pace)
* cycling with fixed load (5 minutes)
* standing up from sitting position and sitting down again (x5)
* standing up from supine position
* turning from left to right and back while lying in bed
* raising outstretched arm 90° (x5, standing position)
* eating (5 minutes, sitting position)
* drinking a glass of water
* sleeping (6 hours)
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Can an Actigraph be Used to Predict Physical Function in Intensive Care Patients?
NCT02899208
Exercise Therapy With Risk Factor Management and Life Style Coaching After Vascular Intervention for Patients With Peripheral Arterial Disease
NCT02110251
(Cost) Effectiveness Study of Exercise Therapy in Patients With Peripheral Arterial Disease
NCT00279994
Increasing Risk Perception of Physical Activity Using Patient-targeted Feedback.
NCT02802254
Physical Activity on Heart Rate Variability in Patients With Severe Acquired Brain Injury
NCT03328221
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.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Transient Ischemic Attack Patients
Patients discharged after a Transient Ischemic Attack
Standardized activities
All patients do each of the following standardized activities over a course of 2 days:
* treadmill walking (5 minutes, 1 and 2km/h)
* staircase walking (1 floor, normal pace)
* cycling with fixed load (5 minutes)
* standing up from sitting position and sitting down again (x5)
* standing up from supine position
* turning from left to right and back while lying in bed
* raising outstretched arm 90° (x5, standing position)
* eating (5 minutes, sitting position)
* drinking a glass of water
* sleeping (6 hours)
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Standardized activities
All patients do each of the following standardized activities over a course of 2 days:
* treadmill walking (5 minutes, 1 and 2km/h)
* staircase walking (1 floor, normal pace)
* cycling with fixed load (5 minutes)
* standing up from sitting position and sitting down again (x5)
* standing up from supine position
* turning from left to right and back while lying in bed
* raising outstretched arm 90° (x5, standing position)
* eating (5 minutes, sitting position)
* drinking a glass of water
* sleeping (6 hours)
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* age \> 18 years
Exclusion Criteria
* time limit of more than 2 days of standardized activities exceeded
* no informed consent
* disability when tested with Scandinavian Stroke Scale (score \<58), National Institutes of Health Stroke Scale (score \>0), modified Rankin Scale (score \>0) and Barthels Index 100 (score \<100)
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hillerod Hospital, Denmark
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Anna Maria Strømmen
principal investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Neurologic Department, Hillerød Hospital
Hillerød, , Denmark
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
H-1-2012-001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.