Condition: Head and Neck Cancer · Sponsor: Uppsala University
The aim of this randomized controlled trial is to investigate the effects of internet-based support (Carer eSupport) on preparedness for caregiving in informal caregivers of patients with head and neck cancer. The main question\[s\] it aims to answer are: * What are the effects of internet-based support on informal caregivers preparedness for caregiving? * What are the effects of internet-based support on informal caregivers burden and wellbeing? Informal caregivers who are randomized to Carer eSupport will have access to Carer eSupport for 18 weeks and they will be asked to complete questionnaires (outcome measures) at: * baseline (before randomization) * 18 weeks (post-intervention) and at * 3 months after the intervention is completed (long term follow-up). Informal caregivers in the intervention group will be compared to informal caregivers who receive standard care support regarding preparedness for caregiving, caregiver burden and wellbeing.
This description comes directly from the study's public registry record.
Ylva Tiblom Ehrsson, Assoc prof · +46707747712 · ylva.tiblom.ehrsson@uu.se
Birgitta Johansson, Assoc prof · birgitta.johansson@igp.uu.se
Always discuss trial participation with your own doctor first.
| Örebro University Hospital | Örebro, Blekinge Län, Sweden | Recruiting |
| Uppsala university hospital | Uppsala, Uppsala County, Sweden | Recruiting |
| Norrland University Hospital | Umeå, Västerbotten County, Sweden | Recruiting |
| Sahlgrenska university hospital | Gothenburg, Västra Götaland County, Sweden | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT06307418