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Supporting Women With Breast Cancer to Practice DIBH at Home Before Radiation Therapy — DIBHApp  

Distress, Emotional Clinical Trial

Official title:
Supporting Women With Left Sided Breast Cancer to Practice Deep Inspiration Breath Hold (DIBH) at Home Before Radiation Therapy Treatment

Clinical Trial Summary

To examine the effect of a preparatory digital tool including a new instruction for deep inspiration breath hold (DIBH), before start of radiation therapy in women diagnosed with left sided breast cancer, compared with usual care.

Clinical Trial Description

The following questions will be posted: - Are there any differences in levels of distress (primary outcome) between the control and intervention group at baseline and over time? - Are there any differences in preparedness for RT (secondary outcomes) between the control and intervention group at baseline and over time? - Are there any correlations between Health Literacy (HL) levels (secondary outcome) and levels of distress (primary outcome) in the control and intervention group? - Are there any differences in objective clinical variables (chest mobility and respiratory movements and planned absorbed dose to the heart) between the control and intervention group before and after the intervention (baseline and at planning CT)? - Which patterns of practice and use of the application (when, how, how often and for how long) can be discerned from the intervention group? - Are there any correlations between different levels of practice and use of the digital tool and primary and secondary outcomes? - How do patients in the different groups (control and intervention group) describe their experience of care and information process during RT with DIBH? - Are there differences regarding health economic variables in terms of costs and health care usage (e.g., estimated time for planning and conducting computed tomography (CT), number of scheduled CT examinations) and patient effects (e.g. co-morbidities (heart related), sick leave, and quality-adjusted life year (QALYs) between patients in control- or interventions group? - Are there any differences regarding effects on environmental aspects and costs in the different groups (control and intervention)? ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05791084
Study type Interventional
Source Jonkoping University
Contact maria Brovall, ass prof
Phone +46705501097
Email maria.brovall@ju.se
Status Not yet recruiting
Phase N/A
Start date September 1, 2023
Completion date March 30, 2029
View Details
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