Mindfulness-Integrated Neuropsychotherapy for Traumatic Brain Injury: A Mixed-Methods Evaluation of Cognitive and Psychosocial Recovery

Study acronym: IMENP
StatusCompleted
PhaseNot applicable
Started

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Record History

  1. Minor Study First Submitted
The goal of this clinical trial is to test the effectiveness of Integrative Mindfulness Enhanced Neuropsychotherapy (IMENP) in improving neurocognitive functioning and wellbeing among adults aged 18 to 44 years with mild to moderate Traumatic Brain Injury (TBI). The main questions it aims to answer are: * Does IMENP improve neurocognitive functioning in individuals with mild to moderate TBI? * Does IMENP improve quality of life, and reduce depression and fatigue in individuals with mild to moderate TBI? Researchers will compare participants who receive the 16 session IMENP programme to participants on a waitlist control condition to see if IMENP improves cognitive functioning and overall wellbeing. Participants in the experimental group will: Attend 16 sessions of IMENP delivered twice weekly over three months Complete mindfulness practices, cognitive rehabilitation exercises, and emotional regulation techniques during sessions Complete between session homework tasks including expressive writing, mindful activities, and reflective exercises Be assessed on neurocognitive functioning, quality of life, depression, and fatigue at baseline, post intervention, and one month follow up Participants in the waitlist control group will: Receive treatment as usual during the three month intervention period Be assessed at the same time points as the experimental group Receive three introductory IMENP sessions following study completion
Trial Details
NCT Number NCT07874685
Lead Sponsor University of Madras
Collaborators: Keele University
Conditions
(from sponsor)
Traumatic Brain Injury (TBI) Patients, Cognitive Impairment, Depression Disorder, Fatigue Severity Scale, Quality of Life (QOL)
Related terms Brain Injuries, Traumatic, Cognitive Dysfunction, Depression, Fatigue
Enrollment 68 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov