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Actigraphic Measurement of a Neurosurgical Procedure

Analysis of Post Surgical Response in A Fifty-Six Year Old Female With An Incidental Large Left Anterior Cranial Fossa Meningioma

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00945230
Enrollment
1
Registered
2009-07-24
Start date
2009-03-31
Completion date
2009-06-30
Last updated
2009-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Circadian Rhythm, Mood Lability, Pain, Rehabilitation, Sleep Disorders

Keywords

Neurosurgical outcome, Actigraphy, Treatment Response Measurement

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.

Interventions

PROCEDURERe-section of a large left anterior cranial fossa meningioma

Neurosurgical re-section of an incidental large left anterior cranial fossa meningioma

Sponsors

Mayo Clinic
CollaboratorOTHER
Child Psychopharmacology Institute
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* Inability to wear actigraphy device

Design outcomes

Primary

MeasureTime frame
Pre and Post Actigraphic and Systematic Observation Scale measurementsMarch 15, 2009-June 20, 2009

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026