Health Expectations: Vol 28, No 3

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Health Expectations: Volume 28, Issue 3

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ISSUE INFORMATION

Issue Information

ORIGINAL ARTICLE

The Coproduced Youth Priorities Project: Australian Youth Priorities for Mental Health and Substance Use Prevention Research

‘The Second Arrow’: A Collaborative Autoethnographic Exploration of What Can Be Learned From One Long COVID Journey

‘I Have Never Been in That Kind of All-Consuming Pain … I Did Not Know What Else to Do’: The Journey to Hospital Admission With Low Back Pain From the Perspectives of Patients

REVIEW ARTICLE

Experiences and Perceptions of Self-Harm in Rural-Dwelling Adults: A Rapid Review of Qualitative Evidence

ORIGINAL ARTICLE

Patient and Clinician Perspectives on Communication in Primary Care Centres in Qatar—A Focus Group Study

Multimodal Analysis of Stories Told by Mental Health Influencers on TikTok

Synergies, Discrepancies, and Action Priorities: A Statewide Engagement Study to Strengthen Clinical Research in Cerebral Palsy

Stakeholder Involvement in the Development of a New Proactive Clinical Review of Patients Prescribed Opioid Medicines Long-Term for Persistent Pain in Primary Care

Digital Long Covid Communities—Shaping Diagnoses, Treatment Strategies and Modes of Expertise

‘They Were Talking to Each Other but Not to Me’: Examining the Drivers of Patients' Poor Experiences During the Transition From the Hospital to Skilled Nursing Facility

Consumers' Contribution to Health Research: Australian Research Organisations' Perspectives

Adapting Experience-Based Co-Design to Disability Research: Co-Producing the CycLink Co-Design Study

Understanding Barriers to Engagement With a Prostate Cancer Research and Genetic Risk Service Among UK Men of Black African or Black Caribbean Ancestry

Correction(s) for this article

Correction to “Understanding Barriers to Engagement With a Prostate Cancer Research and Genetic Risk Service Among UK Men of Black African or Black Caribbean Ancestry”

Perceptions and Experiences of a Multimodal Rehabilitation Program for People With Post-Acute COVID-19: A Qualitative Study

Evaluating the Involvement of People With Cancer and Informal Caregivers in the Development Process of a New Set of Quality of Life Questionnaires

Co-Producing Resources to Help Improve Access to Primary Care for Young People With Attention Deficit Hyperactivity Disorder

Perceptions and Experiences of Consumer Representatives on Patient Safety Investigation Teams: A Qualitative Analysis

Personalisation at the Core of Success: Process Evaluation of the LISTEN Randomised Controlled Trial Evaluating a Personalised Self-Management Support Intervention for People Living With Long Covid

From Doubt to Diagnosis: Canadian Patient Perspectives on a Limb-Girdle Muscular Dystrophy Diagnosis

Illness Expectations and Asthma Symptoms: A 6-Month Longitudinal Study

Addressing the Health Needs of Underserved Populations Through Public Contribution: Prioritisation and Development of a Peer Support Intervention for Sexual and Gender Minority Forced Migrants

Long Covid Symptom Clusters, Correlates and Predictors in a Highly Vaccinated Australian Population in 2023

Families' Perceptions of Powered Mobility for Participation in Children With Spinal Muscular Atrophy Type 1: A Photovoice Study

Implementation, Processes and Outcomes of Advance Care Planning: A Culturally and Contextually Appropriate Programme Theory Developed in Chinese Long-Term Care Facilities

REVIEW ARTICLE

Reimagining Dementia Care: A Complex Intervention Systematic Review on Optimising Social Prescribing (SP) for Carers of People Living With Dementia (PLWD) in the United Kingdom

ORIGINAL ARTICLE

Reporting on a Partnership to Co-Design a Digital Health Intervention With Young People Who Have Experienced Technology-Assisted Sexual Abuse

Listening to Women's Voices: A Patient and Public Involvement Exercise Exploring Vulval Reconstructive Surgery for UK Women With Female Genital Mutilation (FGM)

REVIEW ARTICLE

Reimagining Dementia Care: A Complex Intervention Systematic Review on Optimising Social Prescribing (SP) for People Living With Dementia (PLWD) in the United Kingdom

ORIGINAL ARTICLE

Living With Long COVID: Everyday Experiences, Health Information Barriers and Patients' Quality of Life

Children and Young People's Priorities for Mental Health Research in Northern Ireland

Time for a New Norm: Experiences of ‘Being Informed’ and ‘Having Choice’ for Prenatal Screening for Chromosomal Conditions: A Qualitative Study

REVIEW ARTICLE

Perceptions of Hospital Care Quality According to People Living With Multiple Long-Term Conditions: A Scoping Review

ORIGINAL ARTICLE

Development and Psychometric Testing of EPAT-16: A Short and Valid Measure for Patient-Centeredness From the Patient's Perspective

REVIEW ARTICLE

‘Before and After’. The Journey of Patients With Low Back Pain Consulting in Elective Spine Surgery Clinics. A Qualitative Study Protocol

ORIGINAL ARTICLE

Improving Diversity in Recruitment: Lessons Learned During the REACH Pregnancy Circles Pilot Trial

‘All I Do Is Sit in a Chair Until the Pain Fades’—Experiences of Living With Gout

Processes Underpinning Successful Co-Design: Lessons From a Digital Health Project

Co-Designing a Digital Stroke Prevention Platform: Leveraging Lived Experience and Expert Advice

REVIEW ARTICLE

Understanding Inclusion and Participation of People From Black African Diaspora Communities in Health and Care Research: A Realist Review

ORIGINAL ARTICLE

Anticipating the Future in an Uncertain Present: How Individuals Living With Medically Unexplained Cognitive Complaints Value Biomarker-Based Prognostics

Barriers to Care for Adults With Sickle Cell Disease: A Qualitative Descriptive Study

Protocol for the Process Evaluation of the SENSE-Cog Sensory Support Intervention Field Trial to Improve Quality of Life for Older People Receiving Home Care in Australia

A Mixed-Methods Study Exploring the Feasibility of a Digital Combined Lifestyle Intervention for Patients With Post Covid-19 Condition

Consumers' Perspectives on the Design of a New Digital Frailty Education Course, ‘Focus on Frailty’: A Qualitative Co-Design Study

Developing an Inclusive Dance Guide for Children With Cerebral Palsy: A Co-Design Process and Initial Feasibility Study

Co-Producing and Evaluating a Culturally Inclusive Dementia Education Initiative: A Multimethod Study Protocol

REVIEW ARTICLE

Collaborating With Young People: Identifying the Barriers and Facilitators in Co-Designed Research

ORIGINAL ARTICLE

What Is Important to Older People When Accessing Urgent Health Care: Key Considerations and Recommendations From Consumer Consultations

Improving How Healthcare Staff Support the Psychological Well-Being of People Living With Post-Stroke Aphasia: A Co-Created Study

Recognising Consumers' Contributions to Health Research: Co-Designing a Remuneration Framework for the Australian Context

A Qualitative Study to Improve How We Partner With Patients and Families in Healthcare Improvement Collaboratives

Perceptions and Significance of Long Covid Diagnoses From the Perspectives of Children and Young People With Long Covid, Their Parents and Professionals

Operationalising Patient Engagement Through the Alberta Cancer Diagnosis Initiative: Recruitment Strategies for Diverse Populations in Health System Improvement

‘Nobody Has Ever Spoken to Me About PCD and Fertility Issues’: Fertility Experiences of People With Primary Ciliary Dyskinesia and Their Family Caregivers

Codesigning Solutions for Assistive Technology Service Provision in Queensland, Australia