Effects of Biofeedback in Patients With Acute Cerebral Infarction

NACompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

November 9, 2015

Primary Completion Date

June 26, 2016

Study Completion Date

August 3, 2016

Conditions
Acute Ischemic StrokeBiofeedbackAutonomic Dysfunction, Cognitive FunctionPsychological Distress
Interventions
BEHAVIORAL

heart rate variability biofeedback

The HRVBF group received four, one-on-one bedside biofeedback training sessions (20-minutes a day for 4 days), and practiced on their own (10-minutes twice a day) using a FDA-regulated, hand-held mobile biofeedback device (StressEraser, Helico Inc., New York, NY, USA).26 The control group received usual care.Afterwards, all participants were telephoned bi-weekly and encouraged to practice slow breathing (HRVBF group) or to perform self-care (control group) for three months.

All Listed Sponsors
lead

National Defense Medical Center, Taiwan

OTHER

NCT03516227 - Effects of Biofeedback in Patients With Acute Cerebral Infarction | Biotech Hunter | Biotech Hunter