Catherine S Hurt
Biographic Data
| ID | 1562278 |
|---|---|
| NAME | Catherine S Hurt |
| GIVEN NAMES | Catherine S |
| FAMILY NAME | Hurt |
| SIGNATURE | HURT C S |
| AFFILIATIONS | City, University of London |
| ORCID | 0000-0003-1571-0040 |
| VERIFIED | Yes |
| TOTAL WORKS | 5 |
| TOTAL CITATIONS | 5 |
| WORKS AS AUTHOR | 5 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2012 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 1 |
Adapting a Participatory Group Programme for Caregivers of Children with Complex Neurodisability from Low-, Middle-Income Countries to a High-Income Setting
The "Baby Ubuntu" programme is a well-established, low-cost, community-based intervention to support caregivers of children with complex neurodisability, like cerebral palsy, in low- and middle-income country (LMIC) contexts. This process-focused paper describes our utilisation of the ADAPT guidance to adapt "Baby Ubuntu" for use in ethnically and linguistically diverse, and economically deprived urban boroughs in the United Kingdom (UK). The pro…
Identifying barriers to help-seeking for non-motor symptoms in people with Parkinson's disease
Non-motor symptoms of Parkinson's disease have a significant impact on quality of life. Despite this, many non-motor symptoms remain unreported by patients and consequently untreated. This study explored barriers to help-seeking using two theoretical frameworks, the Common Sense Model of illness perception and Theoretical Domains Framework. A total of 20 participants completed semi-structured interviews to explore symptom beliefs and help-seeking…
Examining the effects of adjuvant chemotherapy on cognition and the impact of any cognitive impairment on quality of life in colorectal cancer patients
The result from this study will indicate whether a decline in cognitive functioning can be attributed to chemotherapy or to disease, surgical or some other confounding factor. Identification of risk factors for cognitive deficits may be used to inform targeted interventions, in order to improve QoL and help patients' cope
Measuring Illness beliefs in neurodegenerative disease
Positive perceptions of illness are typically associated with good health outcomes. However, this may not be true for all domains of illness perception in neurodegenerative diseases because of their progressive incurable nature. The appropriateness of current measures of illness belief in these conditions is not known. The validity and reliability of the Illness Perception Questionnaire-Revised was evaluated in 215 participants with Parkinson's d…
The relationship of depression and disease stage to patient perceptions of Parkinson's disease
The present study aimed to perform an in-depth exploration of perceptions of Parkinson's disease (PD) and their relationship to depression and disease stage using semi-structured interviews. 37 participants with PD formed four groups: depressed and non-depressed with either mild or moderate-severe stage PD. Interviews were analysed using Framework Analysis. Moderate-severe stage patients reported a greater variety of perceptions than those with m…
The relationship of depression and disease stage to patient perceptions of Parkinson's disease
The present study aimed to perform an in-depth exploration of perceptions of Parkinson's disease (PD) and their relationship to depression and disease stage using semi-structured interviews. 37 participants with PD formed four groups: depressed and non-depressed with either mild or moderate-severe stage PD. Interviews were analysed using Framework Analysis. Moderate-severe stage patients reported a greater variety of perceptions than those with m…
Measuring Illness beliefs in neurodegenerative disease
Positive perceptions of illness are typically associated with good health outcomes. However, this may not be true for all domains of illness perception in neurodegenerative diseases because of their progressive incurable nature. The appropriateness of current measures of illness belief in these conditions is not known. The validity and reliability of the Illness Perception Questionnaire-Revised was evaluated in 215 participants with Parkinson's d…
The relationship of depression and disease stage to patient perceptions of Parkinson's disease
The present study aimed to perform an in-depth exploration of perceptions of Parkinson's disease (PD) and their relationship to depression and disease stage using semi-structured interviews. 37 participants with PD formed four groups: depressed and non-depressed with either mild or moderate-severe stage PD. Interviews were analysed using Framework Analysis. Moderate-severe stage patients reported a greater variety of perceptions than those with m…
Examining the effects of adjuvant chemotherapy on cognition and the impact of any cognitive impairment on quality of life in colorectal cancer patients
The result from this study will indicate whether a decline in cognitive functioning can be attributed to chemotherapy or to disease, surgical or some other confounding factor. Identification of risk factors for cognitive deficits may be used to inform targeted interventions, in order to improve QoL and help patients' cope
Measuring Illness beliefs in neurodegenerative disease
Positive perceptions of illness are typically associated with good health outcomes. However, this may not be true for all domains of illness perception in neurodegenerative diseases because of their progressive incurable nature. The appropriateness of current measures of illness belief in these conditions is not known. The validity and reliability of the Illness Perception Questionnaire-Revised was evaluated in 215 participants with Parkinson's d…
Identifying barriers to help-seeking for non-motor symptoms in people with Parkinson's disease
Non-motor symptoms of Parkinson's disease have a significant impact on quality of life. Despite this, many non-motor symptoms remain unreported by patients and consequently untreated. This study explored barriers to help-seeking using two theoretical frameworks, the Common Sense Model of illness perception and Theoretical Domains Framework. A total of 20 participants completed semi-structured interviews to explore symptom beliefs and help-seeking…
Adapting a Participatory Group Programme for Caregivers of Children with Complex Neurodisability from Low-, Middle-Income Countries to a High-Income Setting
The "Baby Ubuntu" programme is a well-established, low-cost, community-based intervention to support caregivers of children with complex neurodisability, like cerebral palsy, in low- and middle-income country (LMIC) contexts. This process-focused paper describes our utilisation of the ADAPT guidance to adapt "Baby Ubuntu" for use in ethnically and linguistically diverse, and economically deprived urban boroughs in the United Kingdom (UK). The pro…
Medicine (5 works) · Psychology (5 works) · Autism Spectrum Disorder Research (4 works) · Clinical Psychology (4 works) · Psychiatry (4 works) · Disease (3 works) · Parkinson's disease (3 works) · Parkinson's Disease Mechanisms and Treatments (3 works) · Perception (3 works) · Cognition (2 works)