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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00370929
Other study ID # HSPC-06-03-001
Secondary ID
Status Completed
Phase N/A
First received August 30, 2006
Last updated July 20, 2016
Start date May 2006
Est. completion date January 2008

Study information

Verified date July 2016
Source University of California, Los Angeles
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Epileptic seizures may occur at times of stress and commonly increase life stress. This study will evaluate whether meditation improves seizure control and quality of life for individuals with uncontrolled epilepsy.


Description:

Individuals who have uncontrolled epilepsy commonly experience disability, depression, anxiety and injuries from seizures. For such individuals, ideal treatments should improve quality of life through control of seizures and improved emotional state. Meditation with cultivation of emotional balance is known to improve emotional state and may also benefit seizure control in some individuals. In this study, individuals with uncontrolled epilepsy will receive detailed training in meditation to determine whether the training leads to improvements in seizure control and various measures of emotion and quality of life.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date January 2008
Est. primary completion date January 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 6 or more seizures per month

- ability to participate in meditation

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Meditation


Locations

Country Name City State
United States Geffen School of Medicine at UCLA Los Angeles California

Sponsors (1)

Lead Sponsor Collaborator
University of California, Los Angeles

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Seizure frequency 20 weeks No
Primary Quality of Life 20 weeks No
Secondary Mood 20 weeks No
Secondary Affect 20 weeks No
Secondary Anxiety 20 weeks No
Secondary Sleep quality 20 weeks No
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