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Stroke clinical trials

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NCT ID: NCT01622205 Enrolling by invitation - Stroke Clinical Trials

GOThenburg Very Early Supported Discharged

GOTVED
Start date: May 2011
Phase: Phase 2
Study type: Interventional

Stroke is a generic term for cerebral infarction and cerebral haemorrhage and accounts for more patient days than any other single condition in Swedish health care. The Swedish guidelines for stroke treatment, issued by the national board for health and welfare, recommend early supported discharge for people with mild to moderate stroke. This is based on studies in which mean hospitalization was 18 days. The average length of stay in Sweden is 12 days. Policy makers would, however, like to shorten length of stay even further, and many patients are anxious to get home. Where and how to get support at home after discharge varies. This study is a randomized controlled trial in which half of the subjects are randomly allocated to very early supported discharge and the other half receives usual treatment. The investigators believe that patients discharged very early with support will experience less anxiety compared with controls. The investigators believe that early supported discharge is safe and that there is no difference between groups in bodily function. In order to test differences between the groups, the study requires approximately 110 subjects. Everyone who comes to the stroke unit at the hospital with a mild to moderate stroke can be recruited to the study. The intervention is having a team from the stroke unit visiting the patient's home and train him/her according to the individualized goals. The controls are discharged according to routine with support from primary care if needed. Assessments are made by therapists who are not involved in the training upon returning home, at 1 month, 3 to 12 months. The assessments include anxiety, motor activity, gait and balance, and ADL. Interviews will be done to highlight the subject's own experience. It is important to evaluate new methods and organizational changes prior to their implementation in health care. The investigators hope to show that very early supported discharge with rehabilitation is safe and provides confidence and less anxiety. Then it is possible to introduce a method that simultaneously improves patient outcome and increases availability of hospital beds.

NCT ID: NCT01511796 Enrolling by invitation - Stroke Clinical Trials

Examining the Effectiveness of Combined Rehabilitation and Botulinum Toxin Injection on Functional Improvement of the Upper Limb After Stroke

Start date: January 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to examine the effects of a combination of "Botulinum Toxin (BT) and Upper Limb (UL) rehabilitation" compared to "BT only" on UL motor function in adults with spasticity after stroke using a pre-post design. The research question is whether combination of BT and UL rehabilitation compared to BT only is more effective in improving the UL function, range of motion and pain.

NCT ID: NCT01234844 Enrolling by invitation - Clinical trials for Cerebrovascular Accident

The Relationship Between Pet Therapy and "Well-being" in Geriatric Rehabilitation In-patients

Start date: November 2010
Phase: N/A
Study type: Interventional

In -patients in a geriatric rehabilitation unit, will participate in structured therapy with guinea-pigs on the assumption that the therapy will reduce anxiety and improve the outcome of their rehabilitation.

NCT ID: NCT01070459 Enrolling by invitation - Clinical trials for Cerebrovascular Accident

The Effect of an Aerobic Exercise Programme in Stroke Patients

Start date: February 2010
Phase: Phase 3
Study type: Interventional

This study aims to investigate the effect of aerobic exercise on the aerobic capacity, the daily functioning, post-stroke fatigue , depression and cardiovascular risk factors in stroke patients.

NCT ID: NCT00776048 Enrolling by invitation - Stroke Clinical Trials

Validation of an Obstacle Course Used in Patients With Muscle Tightness

Start date: January 2007
Phase: N/A
Study type: Observational

This study is being conducted to compare healthy patients versus patients with muscle tightness in their leg(s) after an acquired brain injury using walking trials time, a balance test, and foot pressure data. This data is obtained using foot pressure sensors, timers, and distance walked.