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Early Intervention With a Low-intensity Leg Cycling Exercise Program for Individuals After Stroke

Early Intervention With a Low-intensity Leg Cycling Exercise Program for Individuals After Stroke

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02437006
Enrollment
120
Registered
2015-05-07
Start date
2014-03-31
Completion date
2017-03-31
Last updated
2015-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

stroke, exercise capacity

Brief summary

This is a two-stage study. In the first stage, 30 subjects with stroke (onset \> 2 weeks) are recruited, and they are assessed and recorded with clinical characteristics, sympathetic nerve testing, and twice symptom-limit exercise capacity tests. The second stage would recruited 90 subjects with stroke (onset\>2 weeks), and they are randomized to one of three groups (control, low-intensity, high-intensity). They are evaluated before and after the four-week interval with clinical characteristics and twice symptom-limit exercise capacity tests (baseline and after four-week training) .

Detailed description

This is a two-stage study. In the first stage, 30 subjects with stroke (onset \> 2 weeks) are recruited, and they are assessed and recorded with sympathetic nerve testing, anthropometry, and twice symptom-limit exercise capacity tests.The second stage would recruited 90 subjects with stroke (onset\>2 weeks), and they are randomized to one of three groups. The control group undergoes traditional rehabilitation only, The low-intensity exercise group receives a low-intensity four-week cycle ergometry and traditional rehabilitation. The The high-intensity exercise group gets a high-intensity four-week cycle ergometry and traditional rehabilitation. They are evaluated by sympathetic tests, anthropometry, functional scales and activity questionnaires, and symptom-limit exercise capacity tests before and after the four-week training.

Interventions

OTHERexercise

cycle ergometry

Sponsors

Kaohsiung Medical University Chung-Ho Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* stroke onset longer than two weeks, * eligible for exercise testing by Doctor

Exclusion criteria

* aphasia, * apraxia

Design outcomes

Primary

MeasureTime frameDescription
change values of symptom-limit exercise capacitybaseline and after four-week trainingvalue was showed by oxygen uptake (mL/kg/min)

Secondary

MeasureTime frameDescription
change values of sympathetic nerve testsbaseline and after four-week trainingchange value was measure by blood pressure (from lying to stand, mm-Hg) at baseline and after four weeks

Countries

Taiwan

Contacts

Primary ContactMiao-Ju Hsu, PHD
mjhsu@kmu.edu.tw88673121101

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026