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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02717715
Other study ID # VG 023-15
Secondary ID
Status Completed
Phase N/A
First received March 5, 2016
Last updated July 18, 2017
Start date March 2016
Est. completion date April 2017

Study information

Verified date July 2017
Source Katholieke Universiteit Leuven
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to determine the effect of a supervised home-based physical fitness program on the aerobic capacity, quality of gait and health related quality of life in people with chronic ischemic stroke. Secondly, feasibility of the program for implementing a long term lifestyle change will be investigated.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date April 2017
Est. primary completion date April 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- ability to give informed consent

- ability to understand measurement procedures defined as MMSE >24

- last stroke >6 months ago

- mild to moderate stroke deficit defined by Fugl Meyer test score of 27 to 90 for upper and lower extremities

- FAC =3

- medical clearance to participate in a moderate exercise program

- living at home and having a minimum of 5 stairs at home

Exclusion Criteria:

- serious cardiac condition

- other serious end organ damage

- other neurological deficits leading to disability

- uncontrolled blood pressure (systolic pressure >140, diastolic pressure >90)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Home base stroke rehabilitation
The intervention consists of physiotherapy exercises targeting functional and physical capacity.

Locations

Country Name City State
Suriname Anton De Kom University Paramaribo

Sponsors (3)

Lead Sponsor Collaborator
Katholieke Universiteit Leuven Anton De Kom University, VU University of Amsterdam

Country where clinical trial is conducted

Suriname, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in peak oxygen uptake 4 weeks, 8 weeks and 5 months after start of rehabilitation
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