Corinna Bergelt
Biographic Data
| ID | 7532624 |
|---|---|
| NAME | Corinna Bergelt |
| GIVEN NAMES | Corinna |
| FAMILY NAME | Bergelt |
| SIGNATURE | BERGELT C |
| AFFILIATIONS | Universität Hamburg |
| ORCID | 0000-0003-1413-1872 |
| VERIFIED | Yes |
| TOTAL WORKS | 7 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 7 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2008 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 0 |
Exploring burnout and uncertainty in healthcare professionals
Burnout among physicians has gained increasing attention in recent years. This issue arises not only from stressful working conditions and individual factors but also from the correlation between burnout and physicians’ tolerance of uncertainty. This association could be particularly important in the context of rare diseases, which inherently present greater uncertainty. To date, no studies have explored this topic. Our exploratory study aimed to…
Parental cancer
The study shows that a parent's cancer diagnosis in adolescence can significantly impact various aspects of life, and that young people want to be involved in communication about their parents' illness. The findings suggest personalised psychosocial support, especially through peer groups, is effective in supporting adolescents with a parent who has cancer
Experiences and the psychosocial situation of parental caregivers of children with spinal muscular atrophy against the background of new treatment options
Although new treatment options for SMA showed observable effects for most parents, the main caregiver burden and reported symptoms were attributable to the overburdening care tasks. To unburden families, more screening for unmet needs, family-centered help services, professional caregivers, childcare, and sufficient financial support are needed
Experiences of Health Care and Psychosocial Needs in Parents of Children with Spinal Muscular Atrophy
Spinal muscular atrophy (SMA) is a neurodegenerative disorder that is characterized by progressive weakness, respiratory insufficiency, and dysphagia. Due to symptom burden and disease progress, its care management and impact on daily life can severely burden the families of affected children. The objectives of this study are (1) to explore the health care experiences and (2) to investigate the psychosocial needs of the parents of children with S…
Parent-reported health-related quality of life in pediatric childhood cancer survivors and factors associated with poor health-related quality of life in aftercare
Based on the results, it is necessary for health care professionals to consider the differences in parental perceptions regarding children's aftercare after surviving childhood cancer. High risk patients for poor HRQoL should be detected early, and families should be offered support post-cancer diagnosis to protect survivors' HRQoL during aftercare. Further research should focus on characteristics of pediatric childhood cancer survivors and famil…
Families Affected by Parental Cancer
Parental cancer poses major challenges for families with minor children. Due to diagnosis and treatment family life is disrupted. To prevent long-term consequences in all family members and to design needs-oriented family-centered interventions, further understanding of the family's situation including the impact on the children, quality of life levels and the parental psychosocial needs is necessary. This study aims at investigating the impact o…
Quality of life in partners of patients with cancer
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Quality of life in partners of patients with cancer
Families Affected by Parental Cancer
Parental cancer poses major challenges for families with minor children. Due to diagnosis and treatment family life is disrupted. To prevent long-term consequences in all family members and to design needs-oriented family-centered interventions, further understanding of the family's situation including the impact on the children, quality of life levels and the parental psychosocial needs is necessary. This study aims at investigating the impact o…
Experiences of Health Care and Psychosocial Needs in Parents of Children with Spinal Muscular Atrophy
Spinal muscular atrophy (SMA) is a neurodegenerative disorder that is characterized by progressive weakness, respiratory insufficiency, and dysphagia. Due to symptom burden and disease progress, its care management and impact on daily life can severely burden the families of affected children. The objectives of this study are (1) to explore the health care experiences and (2) to investigate the psychosocial needs of the parents of children with S…
Parent-reported health-related quality of life in pediatric childhood cancer survivors and factors associated with poor health-related quality of life in aftercare
Based on the results, it is necessary for health care professionals to consider the differences in parental perceptions regarding children's aftercare after surviving childhood cancer. High risk patients for poor HRQoL should be detected early, and families should be offered support post-cancer diagnosis to protect survivors' HRQoL during aftercare. Further research should focus on characteristics of pediatric childhood cancer survivors and famil…
Experiences and the psychosocial situation of parental caregivers of children with spinal muscular atrophy against the background of new treatment options
Although new treatment options for SMA showed observable effects for most parents, the main caregiver burden and reported symptoms were attributable to the overburdening care tasks. To unburden families, more screening for unmet needs, family-centered help services, professional caregivers, childcare, and sufficient financial support are needed
Exploring burnout and uncertainty in healthcare professionals
Burnout among physicians has gained increasing attention in recent years. This issue arises not only from stressful working conditions and individual factors but also from the correlation between burnout and physicians’ tolerance of uncertainty. This association could be particularly important in the context of rare diseases, which inherently present greater uncertainty. To date, no studies have explored this topic. Our exploratory study aimed to…
Parental cancer
The study shows that a parent's cancer diagnosis in adolescence can significantly impact various aspects of life, and that young people want to be involved in communication about their parents' illness. The findings suggest personalised psychosocial support, especially through peer groups, is effective in supporting adolescents with a parent who has cancer
Medicine (6 works) · Psychosocial (5 works) · Childhood Cancer Survivors' Quality of Life (4 works) · Clinical Psychology (4 works) · Family Support in Illness (4 works) · Psychology (4 works) · Quality of life (healthcare (4 works) · Cancer (3 works) · Clinical Psychology (3 works) · Disease (3 works)