Follow-up of Patients' Physical Activity in Post-hospitalization

Stroke Clinical Trial

— TICAA'DOM  

Official title:

Follow-up of Patients' Physical Activity in Post-hospitalization by Implementation of Systems of Active Monitoring.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01822938
• Other study ID #: I12006 / TICAA'DOM
• Status: Completed
• Phase: N/A
• Start date: May 2013
• Est. completion date: June 2018

Study information

• Verified date: March 2015
• Source: University Hospital, Limoges
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Physical exercise has been identified as a major item of many affecting many chronic diseases and stroke rehabilitation. It contributes to an improvement in the quality of life and to a decrease in the current treatment side-effects and mortality. Stroke in association with an inactive lifestyle lead to a decrease in physical capability and causes problems in daily activities. The physical capacity and the tolerance for exercise fall simultaneously leading to vicious circle of less and less mobility. Therefore, physical activity for the health is a valid and relevant way to improve the quality of life and to recover functional capacity. The aim of the study is the assessment of the effects of a incentive program for physical activity on people following/with stroke.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 84
• Est. completion date: June 2018
• Est. primary completion date: January 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Person having stroke (ischemic or hemorrhagic)

• Whatever the area of stroke

• Person supported by HEMIPASS (monitoring team and home support)

• Stroke less than 6 months

• Patient walking with or without technical or human assistance: FCC score

Exclusion Criteria:

• Disability limiting the gait before the stroke

• Age < 18 years

• Cognitive impairment limiting participation to the program

• Non signature of the consent

• cardiopulmonary pathology which forbid/banned effort

Related Conditions & MeSH terms

• Stroke

Intervention

Other:
• incentive program for physical activity

Locations

Country	Name	City	State
France	University Hospital, Limoges	Limoges

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Limoges

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The distance on the 6 minute walking test (6MWT)		6 minutes
Secondary	Quality of life	EQ-5D	at 0 month, 6 months and 12 months