Study to Validate the Effects of an Outpatient Secondary Prevention Program for Stroke Victims

NACompletedINTERVENTIONAL
Enrollment

109

Participants

Timeline

Start Date

November 30, 2013

Primary Completion Date

October 31, 2020

Study Completion Date

October 31, 2020

Conditions
Cerebrovascular DisordersStrokePrevention
Interventions
BEHAVIORAL

Outpatient secondary prevention program

The comprehensive outpatient program is designed to last for 12 weeks. Participants are treated in groups of 8 or less. Every week there are two days with therapeutic and educational sessions, once with two hours of physical exercise therapy and once with 45 minutes of aerobic ergometer training and one hour of lecture and counseling. On the day with the two hours of physical therapy one of the sessions includes aerobic ergometer training or Nordic walking, and the other session focuses on improvements of fine motor skills, coordination, balance, mobilization, stretching, weight training or breathing. The lectures include three lectures on etiology, diagnosis, treatment and prevention of stroke by a neurologist, one on vascular risk factors by a cardiologist, five on nutrition counseling by nutritionists, two on active and passive smoking cessation and one lecture on psychological coping strategies given by a neuropsychologist.

BEHAVIORAL

Standard treatment by family physician

Standard treatment by family physician.

Trial Locations (1)

3010

Department of Neurology, Bern University Hospital, Bern

All Listed Sponsors
collaborator

Schweizerische Herzstiftung

OTHER

lead

Insel Gruppe AG, University Hospital Bern

OTHER

NCT01924247 - Study to Validate the Effects of an Outpatient Secondary Prevention Program for Stroke Victims | Biotech Hunter | Biotech Hunter