Sökning: "psychosocial function"
Visar resultat 1 - 5 av 104 avhandlingar innehållade orden psychosocial function.
1. Psychosocial aspects on children with imperforate anus and their parents
Sammanfattning : Aim: The overall aim of this thesis was to explore psychosocial consequences on children with high and intermediate imperforate anus and their parents.Material/Methods: Paper I was an explorative study involving interviews. LÄS MER
2. Quality of Life in Patients with Endocrine Gastrointestinal Tumours
Sammanfattning : The overall aim of this thesis is to investigate health-related quality of life (HRQoL), anxiety and depression in patients with endocrine gastrointestinal (GI) tumours. Patient as well as staff perceptions were assessed. HRQoL was studied with the EORTC QLQ-C30, and anxiety and depression with the Hospital Anxiety and Depression Scale. LÄS MER
3. Psychosocial consequences of high and intermediate imperforate anus
Sammanfattning : Imperforate anus including lack of a normal anorectum is an uncommon malformation. The parents of children born with high and intermediate imperforate anus have to take a big responsibility for the follow-up treatment. It has been revealed that children with imperforate anus have psychosocial problems, though knowledge of this is limited. LÄS MER
4. The Temporomandibular Joint in Juvenile Idiopathic Arthritis : Psychosocial, clinical, imaging and parotid saliva biomarkers
Sammanfattning : Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in children. The disease can affect the temporomandibular joint (TMJ) and cause orofacial growth disturbances, pain, and jaw dysfunction. TMJ arthritis is often asymptomatic and therefore a challenging joint to diagnose. LÄS MER
5. Cancer during Adolescence : Coping Shortly after Diagnosis and Psychosocial Function during the Acute and Extended Phase of Survival
Sammanfattning : In this thesis coping shortly after diagnosis and psychosocial function during the acute and extended phase of survival was investigated for individuals struck by cancer during adolescence. Sixty-one participants were recruited and data were collected from four to eight weeks (T1) up to four years (T7) after diagnosis. LÄS MER