Actigraphic Measurement of a Neurosurgical Procedure

Not Applicable

Completed

• Conditions: Sleep Disorders; Circadian Rhythm; Pain; Rehabilitation; Mood Lability

• Registration Number: NCT00945230
• Lead Sponsor: Child Psychopharmacology Institute

Brief Summary

The study examines and illustrates the utility of utilizing actigraphic measurements to assess treatment response.

Detailed Description

Actigraphic measurements, repeated verbal fluency and multi-symptom operationally defined observations will be recorded for an 11 to 12 day baseline period and continued following neurosurgical tumor resection until a repeat MRI is completed three months after the procedure.

Study Timeline

• Study Start: 2009-03
• Primary Completion: 2009-06
• Study Completion: 2009-06
• Status Verified: 2009-07
• Study First Submitted: 2009-07-23
• Study First Submitted QC: 2009-07-23
• Last Update Submitted: 2009-07-23
• Study First Posted: 2009-07-24
• Last Update Posted: 2009-07-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 1

Inclusion Criteria

• Diagnosis of incidental meningioma
• Single subject preparing to receive neurosurgical intervention

Exclusion Criteria

• Inability to wear actigraphy device

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Pre and Post Actigraphic and Systematic Observation Scale measurements	March 15, 2009-June 20, 2009

Trial Locations

Locations (1)

Child Psychopharmacology Institute; 🇺🇸 Fargo, North Dakota, United States