This review aims to synthesise published evidence on parents'/carers' perspectives regarding the development and content of interventions for children and young people (CYP) with acquired brain injury (ABI) and their families.

This study explores service providers' perspectives on factors limiting ART adherence among persons with disabilities living with HIV in Nigeria (PWDLWHIV). It argues that adherence is hindered by stigma, prejudiced views from service providers, and insufficient tailored programming for PWDLWHIV in the HIV response.

Children and adolescents with chronic pain experience lasting impacts on quality of life, often persisting into adulthood. Inadequate lifestyle factors (LSFs) such as physical inactivity, stress, poor sleep, and unhealthy nutrition can worsen pain severity. This scoping review assesses the extent to which LSFs are addressed in pediatric pain education materials and provides recommendations.

Little is known about the perspectives of prosthesis users and funders regarding the outcomes that are most important when receiving/funding a lower-limb prosthetic intervention.

People with stroke aphasia are often excluded from studies of depression because of their language difficulties. Research on individuals without aphasia suggests that different individuals' experiences with depression can impact their depression management. We conducted a qualitative study to explore experiences with depression as viewed by people with aphasia, their care partners, and speech-language pathologists (SLPs).

This qualitative study explored how participation in a peer support group influences the internalization of stigma, stigma management, and social identity among people with brain injury.

Duchenne muscular dystrophy (DMD) is a progressive neuromuscular disorder causing muscle degeneration, mobility loss, and respiratory decline. Telerehabilitation (TR) may improve access to physiotherapy.

To determine the barriers, enablers and preferences for engagement in early mobilisation from the perspective of aneurysmal subarachnoid haemorrhage (aSAH) survivors in acute and intensive care settings.

Loneliness is a long-term concern in populations with acquired brain injury (ABI). There lacks a consensus on conceptualisation of loneliness and factors contributing to it following brain injury. This systematic review aimed to provide the first comprehensive understanding of loneliness in brain injury, grounded in the lived experience of survivors.

To explore (1) current reablement practice for community-dwelling people living with cognitive impairment or dementia, and (2) allied health practitioner perspectives around implementing reablement.

Aggression and offending can be common after Acquired Brain Injury (ABI). This may be partly attributed to ineffective community-based rehabilitation for health and social needs related to these behaviours. As practitioner perspectives can elucidate the realities of service provision and barriers in rehabilitation, the aim of this study was to explore their perspectives on the effectiveness of rehabilitation for persons with ABI.

To examine the experiences, challenges, and recommendations of Canadian Rehabilitation Providers delivering care to people with Long COVID (PWLC), with the goal of informing best practices and guiding service and policy improvements.

Persistent Postural Perceptual Dizziness (PPPD) is a functional neurologic disorder requiring a multidisciplinary approach combining education, vestibular and physical rehabilitation, cognitive-behavioral strategies, and relaxation. Coordinating such interventions in outpatient care is challenging. This study evaluated whether a short, intensive inpatient rehabilitation program could improve postural control, mobility, and disability in PPPD.

Reducing sedentary behaviour may be an intervention target to improve cardiovascular health in individuals with spinal cord injury. The aim of this study was to systematically review the effects of interventions on sedentary behaviour and cardiovascular disease biomarkers in individuals with paraplegia.

People with cerebral palsy (CP) often experience significant barriers to accessing dental care, yet this area remains under researched in Australia. This study explored how people with CP and their caregivers experience dental services in Australia.

Acquired brain injury (ABI) profoundly impacts the whole family. This study explores family identity using a relational, strengths-focused framework to understand how families navigate ABI together.

To provide a summary of assessments and interventions used to target safer mobility behaviour for fall prevention in older adults and people with Parkinson's disease (PwPD).

To identify barriers to, and initiatives for, access to stroke rehabilitation in Southeast Asia (SEA).

This pilot randomized clinical trial (RCT) evaluated the feasibility and exploratory effects of a mindful parenting participation program integrated into occupational therapy (OT) to enhance parental engagement in the self-care co-occupation of autistic children.

Subacromial pain syndrome (SAPS) is a common musculoskeletal condition compromising physical function. Exercise-based care is first-line treatment, but adherence is compromised. This calls for action to optimize the context for clinical pathways to enhance adherence.

Using a mixed methods study to explore the level of parents' decisional conflict and decision-making experiences when offered hip surgery for their child with non-ambulant cerebral palsy (CP).