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Digital Information Provision in the Perioperative Period of Oesophagus Cancer Patients

Digital Information Provision in the Perioperative Period of Oesophagus Cancer Patients - DIGI-S

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON57801
Enrollment
60
Registered
2025-03-10
Start date
2025-06-19
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Oesophagus carcinoma

Interventions

The control group will receive the patient information folder as is currently standard within the hospital, in which all information is provided on paper. The intervention group will not receive inf

Sponsors

Catharina-ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: -Age > 18 years -Speak fluently Dutch -Diagnosed with oesophageal cancer and elibible for curative treatment (chemotherapy or chemoradiation therapy, if needed followed by oesophageal resection) -Patients possess a tablet or smarthphone on which the 'Thuismeten app' can be installed -Able to provide informed consent

Exclusion criteria

Exclusion criteria: -Patients who are not eligible for curative intend or who eventually do not undergo oesophageal resection -Patients who have no possibility to receive information digitally and/or have limited digital skills.

Design outcomes

Secondary

MeasureTime frame
Secundary outcomes are: -Compliance (VO2 max, handgrip strength, body weight) -Length of hospital stay after oesophageal resection -30-day readmission rates -30- and 90-day complications -Adherence to post-operative protocol -Usability and satisfaction with the app (only for intervention group) -Use of the app (only for intervention group) -Outpatient visits (within study period) -Telephone consultations (within study period)

Primary

MeasureTime frame
The primary outcome of this study is the information satisfaction of patients regarding the method of information provision.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)