← Back to Clinical Trials
Recruiting NCT06490393

NCT06490393 The Impact of Supervision by a Health Care Professional on Quality of Life Questionnaire

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06490393
Status Recruiting
Phase
Sponsor St. Claraspital AG
Condition Health-related Quality of Life
Study Type OBSERVATIONAL
Enrollment 200 participants
Start Date 2024-04-17
Primary Completion 2026-05-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Questionnaires

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 200 participants in total. It began in 2024-04-17 with a primary completion date of 2026-05-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Effect of supervision on scoring and completion on Quality of Life Questionnaire

Eligibility Criteria

Inclusion Criteria: * Patient is ≥18 years of age and legally competent * Signed informed consent available * Systemic oncologic treatment (e.g. chemotherapy, immunotherapy, endocrine therapy) * Current systemic therapy started at least 4 weeks before randomization and is scheduled to continue for at least another 4 weeks after randomization in the same dose and interval * Patient is ready and able to complete quality of life questionnaires in German (on paper Exclusion Criteria: * One or more of the inclusion criteria not met.

Contact & Investigator

Central Contact

Diana de Jong-Bakker

✉ diana.bakkerdejong@claraspital.ch

📞 +41616853604

Principal Investigator

Diana de Jong-Bakker

PRINCIPAL INVESTIGATOR

St. Claraspital Klinische Forschung

Frequently Asked Questions

Who can join the NCT06490393 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Health-related Quality of Life. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06490393 currently recruiting?

Yes, NCT06490393 is actively recruiting participants. Contact the research team at diana.bakkerdejong@claraspital.ch for enrollment information.

Where is the NCT06490393 trial being conducted?

This trial is being conducted at Basel, Switzerland.

Who is sponsoring the NCT06490393 clinical trial?

NCT06490393 is sponsored by St. Claraspital AG. The principal investigator is Diana de Jong-Bakker at St. Claraspital Klinische Forschung. The trial plans to enroll 200 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology