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Neuroimaging study on imagined and real somatosensory stimulation at acupuncture points in healthy volunteers

Neuroimaging study on imagined and real somatosensory stimulation at acupuncture points in healthy volunteers - IMACU

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00036548
Enrollment
24
Registered
2025-04-03
Start date
2025-04-03
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Basic science

Interventions

Group 1: The IMACU study is an exploratory functional MRI study aimed at investigating the neural correlates of real and imagined somatosensory stimulation at acupuncture points. Healthy participants
on the second day, only the imagined stimulation is performed. Since three points (an acupuncture point and two control points) are stimulated and imagined, this results in six different interventions

Sponsors

Charité – Universitätsmedizin Berlin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Healthy, consenting participants aged 18 to 50 years 2. Informed consent (both written and oral) 3. Availability to participate in the study sessions 4. Existing health insurance to allow for follow-up in case of incidental findings

Exclusion criteria

Exclusion criteria: 1. Known aphantasia (lack of sensory imagination) 2. Past or current severe neurological and/or psychiatric disorders 3. History of brain injury 4. History of neurosurgical procedures involving the brain 5. Cognitive deficits and severe speech disorders 6. Alcohol or drug dependence 7. Chronic illness (e.g., asthma, diabetes mellitus) requiring regular medication 8. Use of acute medication or drugs during the measurement period 9. Current pregnancy or planned pregnancy during study participation 10. Contraindications for acupuncture (e.g., use of anticoagulants, inflammation at the insertion site) 11. Exclusion criteria for MRI scanning (e.g., metal implants, pacemakers, claustrophobia, hearing loss above 30 dB, tinnitus, etc.) 12. Current participation in another interventional study

Design outcomes

Primary

MeasureTime frame
The main objective of the study is to evaluate whether imagined acupuncture leads to similar changes in brain activity as real acupuncture at an acupuncture point. However, since this is an exploratory study, there is no primary outcome. All outcomes should therefore be considered exploratory.

Secondary

MeasureTime frame
a. Accuracy of the decodings using multivariate pattern analysis (MVPA) of the differences in BOLD activity between the different conditions. b. BOLD activity during imagination and stimulation. c. Self-assessed imagery ability recorded with the self-developed Vividness of Tactile Imagery Questionnaire (VTIQ). d. Perception of the intervention using a self-developed questionnaire for recording sensations based on the MGH Acupuncture Sensation Scale (MASS) (Kong et al., 2007), measured after each intervention.

Countries

Germany

Contacts

Public ContactDaniel Pach

Charité – Universitätsmedizin Berlin

daniel.pach@charite.de+49 30 450529068

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026