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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00179452
Other study ID # 2003P000337
Secondary ID
Status Completed
Phase N/A
First received September 13, 2005
Last updated March 9, 2017
Start date October 2003
Est. completion date October 2008

Study information

Verified date March 2017
Source Beth Israel Deaconess Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To establish the safety and feasibility of having patients with epilepsy perform yoga.


Description:

Subjects will keep logs of seizure frequency prior to, during, and following training in a yoga regimen. Instruction in the yoga regimen will occur at BIDMC, and home practice following classroom instruction will occur as part of the study. Side effects, changes in seizure frequency, and quality of life assessments will be performed.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date October 2008
Est. primary completion date October 2008
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 64 Years
Eligibility Inclusion Criteria:

1. Must be able to give full informed consent.

2. Must have one or more of the following seizure types: simple partial, complex partial, or secondarily generalized.

3. Age 18-64.

4. Must have 4-20 during the baseline phase.

5. Must have medical clearance from their primary care giver sufficient to allow for participation in yoga exercises.

6. Must be stable enough to allow for all anticonvulsant levels to remain constant for the duration of the study.

Exclusion Criteria:

1. Having primary generalized epilepsy or atonic seizures.

2. Having a history of status epilepticus in the past two years.

3. Any medical problem that would preclude participation in a yoga class.

4. Nonepileptic or psychogenic seizures.

5. Pregnancy.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Yoga


Locations

Country Name City State
United States Beth Israel Deaconess Medical Center Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Beth Israel Deaconess Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement in quality of life assessments. 3 months
Primary Improvement in mood. 3 months
Secondary Improvement in seizure control. 3 months
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