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XNKQ Acupuncture Compared to Control Interventions Measured With EEG and fMRI

C

Claudia M. Witt

Status

Completed

Conditions

Stroke

Treatments

Other: Control 2
Other: XNKQ
Other: Control 1
Other: Control 3

Study type

Interventional

Funder types

Other

Identifiers

NCT02453906
XNKQ-15

Details and patient eligibility

About

The investigators will use EEG, structural MRI, and resting-state functional connectivity MRI to assess neuronal responses in 28 healthy subjects to different somatosensory stimulations.

Full description

To develop a better understanding of the cerebral response to a complex somatosensory intervention with XNKQ acupuncture and to build a foundation for future studies with stroke patients our study aims to evaluate changes of brain activity and brain structure in healthy subjects after XNKQ acupuncture in comparison to three control interventions. We will use EEG, structural MRI, and resting-state functional connectivity MRI to assess neuronal responses in 28 healthy subjects to a) strong manual needle-stimulation of the acupuncture points DU26, PC6 and SP6 (XNKQ acupuncture), b) insertion of needles on the acupuncture points DU26, PC6 and SP6 without stimulation (control 1), c) strong manual needle stimulation of three non-acupuncture points (control 2), and d) insertion of needles on three non-acupuncture points without stimulation (control 3). With this, our study aims to create results which inform future studies in patients and might be helpful for the rehabilitation of deficits after stroke.

Enrollment

29 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy subjects (18 to 40 years of age) health status confirmed by a comprehensive neurological examination
  • Right-handed (evaluated by "the Edinburgh inventory")
  • Informed consent
  • No acupuncture treatment in the last 12 months
  • No medical knowledge about acupuncture

Exclusion criteria

  • History of neurological and/or psychiatric diseases
  • History of brain injury
  • Cognitive handicap and severe speech disorder
  • alcohol or drug abuse
  • History of neurosurgical intervention
  • Chronic disease (e.g., asthma, diabetes mellitus etc.) with regular use of medications
  • Usage of acute medication
  • Pregnancy (tested by urine pregnancy test before the measurement) or planned pregnancy
  • Any contraindication for acupuncture (e.g., anti-coagulation therapy)
  • Any exclusion criteria for MRI scanning (metal implants (e.g. pacemaker), claustrophobia, etc.)
  • Participation in another interventional trial.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

29 participants in 1 patient group

healthy subjects
Experimental group
Description:
they receive XNKQ acupuncture, as well as control 1, control 2, and control 3 in a randomized order.
Treatment:
Other: Control 2
Other: XNKQ
Other: Control 3
Other: Control 1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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