ClinicalTrials.Veeva

Menu

The Effect of Acupuncture Treatment on Cognitive Functions and Brain Networks for Long COVID

T

Tingting Luo

Status

Begins enrollment in 2 months

Conditions

Long Covid

Treatments

Other: Sham acupuncture
Other: Acupuncture

Study type

Interventional

Funder types

Other

Identifiers

NCT07355751
2025KL-086

Details and patient eligibility

About

Background of study:

Long COVID(LC) is a prevalent sequalae of SARS-CoV-2 infection and can affect multiple organ systems. Cognitive dysfunction is one of the most common symptoms in LC with 22% prevalence. It can persist for years and significantly reduce patients' quality of life. Brain network is the neural basis underlying human cognitive processes. Diffusion tensor imaging (DTI) and functional magnetic resonance imaging(fMRI) research has revealed that alterations of network characteristics were associated with cognitive impairments across attention, memory, executive function and language in LC. Currently, there is no accepted therapy for cognitive impairment in LC. Acupuncture, as a Traditional Chinese Medicine therapy, has potential to improve cognitive deficits for LC. However, research focusing on the impact of acupuncture on cognitive functions in LC is rare. Additionally, no one has evaluated the mechanism of acupuncture improving cognitive functions in LC.

Objective of the study:

This study aims to assess the effect of acupuncture treatment on cognitive function and explore the central mechanism of acupuncture therapy in improving cognitive function for LC using cognitive assessments, DTI and resting-state fMRI.

Study design:

A prospective, three-armed, randomized controlled trial with DTI and rs-fMRI. Adults with LC will be randomly assigned to acupuncture, sham acupuncture, or waitlist control group in a 1:1:1 ratio, receiving 8-week intervention or waiting. Cognitive function and topological attributes of brain networks will be examined at baseline and 8th week.

Study population:

Patients fulfilling World Health Organization (WHO) criteria for LC will be included in this study.

Enrollment

108 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 18-60 years
  • Fulfilling WHO criteria for long COVID
  • History of confirmed COVID-19 through RT-PCR of nasopharyngeal swab or antigen test of nasal swab ;
  • Having subjective cognitive problems
  • Native Chinese speakers
  • Right handedness
  • Voluntary to participate in the study and signing the informed consent form.

Exclusion criteria

  • Preexisting cognitive symptoms before COVID-19
  • Previous or current diagnosis of chronic conditions that may affect cognitive performances (such as neurological, psychiatric disorders, organ failure, chronic infectious diseases)
  • Prior loss of consciousness
  • History of major surgery within a year
  • Long-term use of drugs that may influence cognition(such as tranquilizer, antidepressant, immunosuppressor)
  • Previous acupuncture treatment within 3 months
  • Involvement of other clinical study within 4 weeks
  • Obesity(BMI≥28)
  • Sensory disorders(deafness, color blindness)
  • Limb dysfunction
  • Metal implantation
  • Claustrophobia
  • Pregnancy or lactation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

108 participants in 3 patient groups

Verum Acupuncture group
Experimental group
Description:
Acupoints with acupuncture treatment
Treatment:
Other: Acupuncture
Sham acupuncture group
Sham Comparator group
Description:
Non-acupoints with sham acupuncture treatment
Treatment:
Other: Sham acupuncture
Waitlist control group
No Intervention group
Description:
Acupoints with acupuncture treatment after 8-week waiting period

Trial contacts and locations

1

Loading...

Central trial contact

Tingting Luo

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems