Home Monitoring During Chemoradiation
Recruiting now
Conditions studied: Locally Advanced Oesophageal Cancer
In brief
Chemoradiotherapy is part of standard treatment for patients with locally advanced oesophageal cancer. Some patients with oesophageal cancer treated with chemoradiotherapy do not complete treatment due to toxicity, or face complications after treatment. Therefore, there is a need for better tools for assessing patients' fitness for chemoradiotherapy and to pick up early signals of deteriorating overall physical condition and complications during and after treatment to timely implement supportive care measures. Tools enabling monitoring physical activity, vital parameters and creatinine concentration in the blood at home are available but have not yet been implemented in patients undergoing chemoradiotherapy for oesophageal cancer. The feasibility and added value remain unknown.
Key facts
- Study ID
- NCT06597240
- Run by
- University Medical Center Groningen
- People needed
- 30
- Starts
- 2025-05-15
- Expected to finish
- 2026-10-01
- Last updated by the study team
- 2025-08-14
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥ 18 at the time of signing informed consent.
- Histologically proven adenocarcinoma, squamous cell carcinoma or mixed type of the oesophagus or gastro-oesophageal junction.
- Indication for definitive or neoadjuvant CRT, with chemotherapy that consists of weekly carboplatin/paclitaxel.
- Written, informed consent.
- Ability to comply with all protocol required actions (at home measurements are done individually by the participant him- or herself).
You may not qualify if…
- Altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent or the carrying out of the measurements at home.
Where it is running
- University Medical Center Groningen — Groningen, Netherlands (enrolling)
Full record on ClinicalTrials.gov
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