Purpose: Identify perceptions of parents and caregivers of children with cerebral palsy about being consumer research partners and identify strategies to inform involvement of parents in cerebral palsy research. Materials and methods: Twenty-two parents in New South Wales and Victoria (Australia) participated in this qualitative study. Seven interviews and three focus groups were completed. Interpretive description guided data analysis. Methodological rigor was enhanced through involving two consumer investigators in the research team, member checking, and multiple researchers completing data analysis and theme generation. Results: Participants identified a range of factors that may influence their involvement in research partner role...
Background: Emotionally available parent–child relationships are supportive of child health and deve...
Understanding the experiences of parents with their child's intervention might help meet the needs o...
OBJECTIVE: To explore the experiences and needs of parents of young children (aged 2-4 years) with c...
Purpose Identify perceptions of parents and caregivers of children with cerebral palsy about being c...
Purpose: Identify perceptions of parents and caregivers of children with cerebral palsy about being ...
Purpose Children and adolescents with cerebral palsy have diverse needs and often engage with health...
Purpose: Children and adolescents with cerebral palsy have diverse needs and often engage with healt...
The purpose of research: To reveal the attitude of parents raising a child with cerebral palsy to re...
This research aims to understand, with the aid of a knowledge broker (KB), how parents use knowledge...
While there is a considerable body of knowledge investigating the efficacy of constraint-induced mov...
Purpose: The purpose of this study was to explore the experience of parents of children with cerebra...
Plain English summary More and more patients and family members are getting involved in health resea...
We share our experiences as academic physical therapists and parents of young people with cerebral p...
The phenomenological approach of qualitative research was used in this study. The participants of th...
With the aim of establishing a foundation for collaboration and partnership in research, parents and...
Background: Emotionally available parent–child relationships are supportive of child health and deve...
Understanding the experiences of parents with their child's intervention might help meet the needs o...
OBJECTIVE: To explore the experiences and needs of parents of young children (aged 2-4 years) with c...
Purpose Identify perceptions of parents and caregivers of children with cerebral palsy about being c...
Purpose: Identify perceptions of parents and caregivers of children with cerebral palsy about being ...
Purpose Children and adolescents with cerebral palsy have diverse needs and often engage with health...
Purpose: Children and adolescents with cerebral palsy have diverse needs and often engage with healt...
The purpose of research: To reveal the attitude of parents raising a child with cerebral palsy to re...
This research aims to understand, with the aid of a knowledge broker (KB), how parents use knowledge...
While there is a considerable body of knowledge investigating the efficacy of constraint-induced mov...
Purpose: The purpose of this study was to explore the experience of parents of children with cerebra...
Plain English summary More and more patients and family members are getting involved in health resea...
We share our experiences as academic physical therapists and parents of young people with cerebral p...
The phenomenological approach of qualitative research was used in this study. The participants of th...
With the aim of establishing a foundation for collaboration and partnership in research, parents and...
Background: Emotionally available parent–child relationships are supportive of child health and deve...
Understanding the experiences of parents with their child's intervention might help meet the needs o...
OBJECTIVE: To explore the experiences and needs of parents of young children (aged 2-4 years) with c...