A rapid realist review of clinical neuropsychology rehabilitation programmes to improve psychological wellbeing and quality of life for people with acquired brain injuries

Neuropsychol Rehabil. 2024 Sep;34(8):1035-1070. doi: 10.1080/09602011.2023.2273580. Epub 2023 Nov 17.

Abstract

Approximately 20% of acquired brain injury (ABI) survivors experience reduced psychological wellbeing (PWB). Neuropsychological rehabilitation (NPR) is one approach supporting people with ABI to participate meaningfully in activities despite challenges. Although literature supports NPR effectiveness, little is known about change mechanisms. This systematic realist review identifies what NPR programmes have been designed, delivered, and evaluated for people with ABI to improve PWB and/or quality of life (QOL), as well as providing a context-relevant understanding of what NPR includes and how NPR might lead to positive outcomes. A rapid realist review was conducted in three phases: (1) structured retrieval and evidence extraction; (2) stakeholder consultation; (3) analysis and synthesis. Searches were completed, and findings from 35 publications and one stakeholder consultation were synthesized into a refined logic model. Six context-mechanism-outcome chains (CMOCs) were identified. Participants' relationships to internal experiences, and feelings of self-worth, mastery, and connection appeared to be mechanisms that led to improved PWB and QOL. Adaptation and individualized programmes were also key mechanisms to explain successful NPR. Embedding CMOCs into NPR could improve PWB and/or QOL for people with ABI. The logic model will inform ongoing development of a new online, group-based, NPR programme.

Keywords: Neuropsychological rehabilitation; acquired brain injury; psychological wellbeing; quality of life; realist review.

Publication types

  • Systematic Review
  • Review

MeSH terms

  • Brain Injuries* / psychology
  • Brain Injuries* / rehabilitation
  • Humans
  • Neurological Rehabilitation*
  • Neuropsychology
  • Quality of Life*

Grants and funding

This work was supported by NIHR Research for Patient Benefit: [Grant Number 202753].