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Epilepsy Surgery and Cognitive Outcome

Epilepsy Surgery and Cognition, Psychiatric Function and Quality of Life - Outcome 10 Years or More After Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04264780
Enrollment
102
Registered
2020-02-11
Start date
2019-08-15
Completion date
2023-10-30
Last updated
2023-11-01

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

Conditions

Epilepsy, Temporal Lobe

Keywords

Epilepsy, surgery, temporal lobe

Brief summary

This study will give important information about long term consequences of temporal lobe epilepsy surgery on cognition (memory, language, concentration etc), psychiatric function and quality of life.

Detailed description

All patients in Norway who have undergone temporal lobe epilepsy surgery ten years ago or more, will be invited to participate. Two groups will be compared: patients who are younger than 50 years of age vs patients who are older than 50 years of age. The aim of the study is to improve preoperative information to future epilepsy surgery patients, to aid medical personnel (doctors, psychologists) in the selection of patients for surgery, and to improve knowledge of need for long term follow-up and rehabilitation.

Interventions

Neuropsychological follow-up examination, including questionaires

Sponsors

Oslo University Hospital
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Prior temporal lobe epilepsy surgery (10 years ago or more)

Exclusion criteria

* Intelligence quotient (IQ) less than 70 * Other main language than Norwegian

Design outcomes

Primary

MeasureTime frameDescription
Change in each study group on neuropsychological tests of memory from baseline (preoperative) to current evaluationDuring single data collection session, aproximately 2 hoursMemory will be measured by Rey Auditory Verbal Learning Test, results reported as raw scores from 1-worst to 15-best; and Diagnosticum für Cerebralschädugung-Revised - DCS-R, results reported as raw scores from 1-worst to 15-best. All results will be converted to T-scores with average 50, standard deviation 10.
Change in each study group on neuropsychological tests of language from baseline (preoperative) to current evaluationDuring single data collection session, aproximately 2 hoursLanguage will be measured by the subtest Similarities from Wechsler Adult Intelligence Scale - WAIS-III, results reported as raw scores from 1-worst to 33-best; Boston Naming Test-results reported as raw scores from 1-worst to 60-best; Letter Fluency from Delis Kaplan Executive Function Scale-D-KEFS, raw scores from 1-worst and up. All results will be converted to T-scores.
Change in each study group on neuropsychological tests of visuospatial abilities from baseline (preoperative) to current evaluationDuring single data collection session, aproximately 2 hoursVisuospatial abilities will be measured by the subtest Block Design from WAIS-III, raw scores from 1-worst to 68-best. Results will be converted to T-scores.
Change in each study group on neuropsychological tests of executive function from baseline (preoperative) to current evaluationDuring single data collection session, aproximately 2 hoursExecutive function will be measured by the subtest Digit Span from WAIS-III, raw scores from 1-worst, to 30-best; Trails A and B from Halstead test battery, raw scores from 1-worst and up. All results will be converted to T-scores.

Secondary

MeasureTime frameDescription
Score on depression questionaireDuring single data collection session, aproximately 2 hoursBeck Depression Inventory (raw scores divided in 4 categories: 0-13 minimal depression, 14-19 mild depression, 20-28 moderate depression and 29-63 serious depression).
Score on anxiety questionaireDuring single data collection session, aproximately 2 hoursBeck Anxiety Inventory (raw scores divided in 4 categories: 0-7 minimal anxiety, 8-15 mild anxiety, 16-25 moderate anxiety and 26-63 serious anxiety).
Score on quality of life inventoryDuring single data collection session, aproximately 2 hoursQuality of Life in Epilepsy - QUOLIE 89 - results will be reported as overall score ranging from 26-worst, to 95-best, and converted to T-score with average 50, standard deviation 10)

Countries

Norway

Outcome results

None listed

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