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Design and Evaluation of Care Environment and Technology at Pediatric Radiotherapy

Design and Evaluation of Care Environment and Technology at Pediatric Radiotherapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02993978
Acronym
DUMBO
Enrollment
57
Registered
2016-12-15
Start date
2012-08-31
Completion date
2015-08-31
Last updated
2016-12-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric ALL, Radiotherapy Side Effect

Keywords

Pediatric radiotherapy

Brief summary

The purpose of the study is to evaluate the effect of changes in the care environment in pediatric radiotherapy. The definitions of the changes is a part of the study, and is constructed in collaboration with the institute of design at Umeå University. The implementation is however not part of the study, but done as part of Clinical routine. The study consist of two parts, where the first 1.5 years are a Control phase where the changes are designed and also function as a baseline period. The following 1.5 years are the case period where the Changes that are accepted for Clinical implementation are implemented. The impact of the changes are evaluated using surveys and interviews of both parents and children

Detailed description

The purpose of the study is to evaluate the effect of changes in the care environment in pediatric radiotherapy. The definitions of the changes is a part of the study, and is constructed in collaboration with the institute of design at Umeå University. The implementation is however not part of the study, but done as part of Clinical routine. The study consist of two parts, where the first 1.5 years are a Control phase where the changes are designed and also function as a baseline period. The following 1.5 years are the case period where the Changes that are accepted for Clinical implementation are implemented. The impact of the changes are evaluated using surveys and interviews of both parents and children. Interviews of the personnel regarding their experiences of the study and the changes is performed after the finalization of the case period.

Interventions

None listed

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Radiotherapy treatment

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Childrens anxiety during treatment period1 dayFAS-evaluation
Parents view of the care and care environmentAfter treatment period (within 2 months after last treatment)Semi structured interview
Childrens reflections regarding the treatment periodAfter treatment period (within 2 months after last treatment)Semi structured interview
Parents anxiety during treatment period1 dayVAS-anxiety scoring in connection to therapy
Parents quality of Life during treatment period1 dayPedsQL survey

Secondary

MeasureTime frameDescription
Experiences of the personnelAfter the case period (within 1 year)Interviews
Use of sedative treatment in connection to radiotherapyup to 2 monthsThe use of sedative treatments were recorded for each fraction

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026