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Recruiting NCT07132034

NCT07132034 Stress Reduction Through Acupuncture

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Clinical Trial Summary
NCT ID NCT07132034
Status Recruiting
Phase
Sponsor Isabell Xiang Ge
Condition Acupuncture
Study Type INTERVENTIONAL
Enrollment 112 participants
Start Date 2026-07-07
Primary Completion 2028-07

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
AcupunctureStandard supportive care

Eligibility Fast-Check

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

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 112 participants in total. It began in 2026-07-07 with a primary completion date of 2028-07.

⚠ 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

This randomized controlled trial evaluates whether eight weeks of weekly acupuncture can reduce psychological distress in breast cancer patients who have recently completed primary therapy compared to standard-of-care wait-list control.

Eligibility Criteria

Inclusion criteria: * Patients with localized breast cancer having completed primary therapy (operation +/- chemotherapy +/- radiotherapy) in the last 6 months - Distress Thermometer ≥ 5 - Age ≥ 18 years - Signed informed consent for participation of the trial * Prior cancer is allowed * Prior treatment - including chemotherapy - for a prior malignant tumor (including breast cancer) is allowed * Concomitant participation in an experimental therapeutic drug trial is allowed * Ongoing or planned Anti-her2/neu, immune checkpoint inhibitor, antihormonal and CDK4/6 inhibitor therapy or other adjuvant treatment scheduled for \> 3 months during study period is allowed * Use of other complementary methods (including mistletoe) is allowed. Exclusion criteria: * Patients with language or cognitive deficits (including impaired consciousness) that are incompatible with the participation in the study * Severe physical or psychiatric comorbidity that prevents a patient from participating in the study * Patients incapable of giving consent * Pregnancy

Contact & Investigator

Central Contact

Isabell Xiang Ge, MD

✉ isabellxiang.ge@usb.ch

📞 +41 61 265 85885

Principal Investigator

Viola Heinzelmann-Schwarz, Prof.MD

STUDY CHAIR

University Hospital of Basel

Frequently Asked Questions

Who can join the NCT07132034 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Acupuncture. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07132034 currently recruiting?

Yes, NCT07132034 is actively recruiting participants. Contact the research team at isabellxiang.ge@usb.ch for enrollment information.

Where is the NCT07132034 trial being conducted?

This trial is being conducted at Basel, Switzerland, Rheinfelden, Switzerland, Thun, Switzerland.

Who is sponsoring the NCT07132034 clinical trial?

NCT07132034 is sponsored by Isabell Xiang Ge. The principal investigator is Viola Heinzelmann-Schwarz, Prof.MD at University Hospital of Basel. The trial plans to enroll 112 participants.

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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: July 2026  ·  Data Methodology