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Rehabilitation Including Social Activity and Education in Children and Teenagers With Cancer

6 Years
18 Years
Open (Enrolling)
Childhood Cancer

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Trial Information

Rehabilitation Including Social Activity and Education in Children and Teenagers With Cancer

Background In Denmark 200 children under the age of 18 are diagnosed annually with cancer
and the prevalence of patients undergoing anticancer therapy is 300. The expected five-year
survival rate is 80%, but since the treatment is intensive with a high risk of
life-threatening infections, these patients are frequently isolated at home or in hospital
during their 1-2 years of therapy, which means reduced contact with their normal school
environment, leisure activities and friends. Long-term survivors of childhood cancer
frequently have compromised age-appropriate social relationships and psychosocial
development, difficulties with resuming physical activities, and poor self-esteem leading to
reduced quality of life. Intervention studies designed to improve physical and social
function during treatment of children with cancer are lacking.

Aim To develop an interactive rehabilitation programme that a) preserve the educational,
physical and psychosocial life of the patients or even obtains "growth with cancer", b)
maintains the child's everyday life (e.g. normal social relationships), and c) improves
long-term physical performance, social competences, higher grade educational enrollment, and
later integration into the labour market.

Theoretical basis This project is inspired by Erving Goffman's interactional theory on
normality and related concepts of stigma and frame analysis as well as Thomas Scheff's
theory on the concept of emotional and social bonds and the development of the sociology of

Material and methods Intervention group: Children aged 6.0-18.0 years diagnosed with cancer
2013-2015 at Rigshospitalet (covers eastern part of Denmark (approximately 50% of total

Control group:

The primary control group is children with cancer treated at the university hospitals in
Odense, Aarhus and Aalborg 2013-2015.

In addition, outcome data for cases will be compared with three other (secondary)
comparative groups: a) children with cancer treated at any Danish childhood oncology unit
throughout Denmark in 2012 (historical controls); b) the sibling closest in age to the
intervention group patients (family matched); and c) the intervention group patient's

Questionnaires: PedsQL, Strength and Difficulties Questionnaire (SDQ), Revised Child anxiety
and Depression Scale, Resilience, Loneliness and Social Dissatisfaction Questionnaire og The
Children´s Impact of Event Scale 13

Qualitative interviews: Qualitative interviews are performed with children with cancer,
their parents, and the ambassadors. The focus will be on sociometric status, social
independence and competences, self-esteem, fatigue, physical activity, educational outcome,
and safety issues as well as an evaluation of the intervention program.

Outcomes and statistical considerations Provided all children with cancer (6-18 years) are
included in the intervention or control group this study will be national cohort study
including approximately 120 intervention children and 120 control children during the three
year intervention period.

If the children´s academic performance are divided into five categories (unsatisfactory to
outstanding level of performance) with a distribution of performance on the five categories
as 10 %; 20 %; 40 %; 20 %; 10 % and where a change from one category to another are regarded
as a significant change in the child´s academic performance, it is possible to achieve a
strength over 0.90 to detect a change of the average by 0.5 if 120 children are included.

Inclusion Criteria:

- Children diagnosed with cancer and treated at the pediatric oncology units in Denmark
(Rigshospitalet, Odense University hospital, Aarhus University Hospital and Aalborg
University Hospital)

Children diagnosed with non-malignant diseases treated with surgery, chemotherapy or
irradiation similar to cancer (e.g. benign CNS tumors, langerhans cell histiocytosis,
Myelodysplastic Syndrome (MDS)) and treated at the pediatric oncology units in Denmark
(Rigshospitalet, Odense University hospital, Aarhus University hospital and Aalborg
University Hospital).

Attend school at the time of diagnosis

Able to communicate in Danish

Exclusion Criteria:

- Mental retardation at the time of diagnosis (including Down syndrome). Terminal
illness at the time of diagnoses. Severe co-morbidity.

Type of Study:


Study Design:

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Outcome Measure:

Level of educational achievement

Outcome Description:

The child´s level of education in Danish (1. language and reading) and math is measured on a five point scale including outstanding level of performance, high level of performance, satisfactory level of performance, needs improvement in level of performance, and unsatisfactory level of performance. Maximum 10% of the children in the intervention group receiving the integrated education program with their regular class mate's will experience a decrease of one or more levels on the five point performance scale.

Outcome Time Frame:

1 year after cessation of first-line cancer treatment

Safety Issue:


Principal Investigator

Kjeld Schmiegelow, M.D

Investigator Role:

Study Director

Investigator Affiliation:

University Hospital of Copenhagen, Rigshospitalet


Denmark: Danish Health and Medicines Authority

Study ID:

RESPECT - education



Start Date:

January 2013

Completion Date:

January 2019

Related Keywords:

  • Childhood Cancer
  • childhood
  • cancer
  • education
  • physical activity
  • quality of life