Viewing Study NCT02692352



Ignite Creation Date: 2024-05-06 @ 8:14 AM
Last Modification Date: 2024-10-26 @ 11:57 AM
Study NCT ID: NCT02692352
Status: COMPLETED
Last Update Posted: 2016-02-26
First Post: 2016-02-23

Brief Title: Cognitive Rehabilitation of Executive Dysfunction - Goal Management Training in Patients With Acquired Brain Injury
Sponsor: Sunnaas Rehabilitation Hospital
Organization: Sunnaas Rehabilitation Hospital

Study Overview

Official Title: Cognitive Rehabilitation of Executive Dysfunction - Goal Management Training in Patients With Acquired Brain Injury
Status: COMPLETED
Status Verified Date: 2016-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The main objective of this study is to examine the effect of Goal Management Training for patients with executive difficulties after acquired brain injury in a randomized controlled trial The effect on cognitive functioning will be examined as will the relationship between treatment effects and lesion location and size The effect of Goal Management training on regulating emotions quality of life and coping will be examined The generalizability of treatment effects across etiologies will be explored by comparing effects in three patient groups traumatic brain injury cerebrovascular accidents and resected brain tumors Structural Magnetic Resonance Imaging MRI scans and measures of white matter connectivity will be used to establish detailed lesion descriptions Functional MRI data will provide information on the neural underpinnings of treatment related change A secondary objective is to expand the Goal Management Training protocol with increased focus on emotional regulation and adherence to homework assignment
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None