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Study on the Correlation Between Neurotrophic Factors and the Condition of Stroke Patients

C

Chongqing Medical University

Status

Enrolling

Conditions

Stroke

Treatments

Procedure: acupuncture
Behavioral: computerized cognitive training system
Behavioral: aerobic exercise
Other: Conventional treatment
Behavioral: tranditional cognitive training

Study type

Interventional

Funder types

Other

Identifiers

NCT05479903
2021kelunshen110

Details and patient eligibility

About

Stroke is currently the most common disabling disease, which often leads to impairment of sensory, motor, speech and psychological functions, resulting in a reduced quality of life for patients. Therefore, post-stroke functional rehabilitation, especially the rehabilitation of physical function and psychological condition, is particularly important for patients to rejoin society. Acupuncture can promote the functional recovery of patients and facilitate the rehabilitation of limb function, thus improving the quality of survival of post-stroke patients.

Neurotrophic factors are diverse, most of which are mainly derived from neuronal cells in the central nervous system and are involved in a variety of neurological functions such as cell growth, differentiation and plasticity, thus promoting recovery of multiple functions after stroke. Many studies have found that different interventions affect the prognosis of stroke patients differently, e.g., long-term acupuncture increases serum levels of brain-derived neurotrophic factor in stroke patients and also has better outcomes than controls in post-stroke neurological recovery and the development of post-stroke psychiatric disorders.

This study investigated the effects of different therapeutic measures on patients' functional recovery and neurotrophic factors by setting up a controlled and blinded trial design, which could not only provide clinical evidence for the effectiveness of relevant therapeutic measures, but also verify the clinical value of certain neurotrophic factors (e.g., predicting outcome, assessing condition, and preventing adverse events).

Enrollment

300 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Symptom recognition to admission ≤ 72 hours
  • Clear imaging evidence
  • Diagnosis of spontaneous cerebral hemorrhage by an immobilized physician according to relevant guidelines; pre-onset mRS score ≤ 1

Exclusion criteria

  • This onset was caused by traumatic and violent factors
  • History of previous intracranial surgery
  • Previous cerebrovascular accident
  • Previous speech disorders and limb movement disorders
  • Participation in other trials in the last three months.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

300 participants in 7 patient groups, including a placebo group

acupuncture stroke group
Experimental group
Treatment:
Procedure: acupuncture
Other: Conventional treatment
sham acupuncture stroke group
Sham Comparator group
Treatment:
Other: Conventional treatment
no acupuncture stroke group
Placebo Comparator group
Treatment:
Other: Conventional treatment
acupuncture healthy group
Placebo Comparator group
Treatment:
Procedure: acupuncture
computerized cognitive training group
Experimental group
Treatment:
Behavioral: computerized cognitive training system
Other: Conventional treatment
tranditional cognitive training group
Placebo Comparator group
Treatment:
Behavioral: aerobic exercise
Other: Conventional treatment
aerobics group
Experimental group
Treatment:
Behavioral: tranditional cognitive training
Other: Conventional treatment

Trial contacts and locations

1

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Central trial contact

Lingcong Li, M.S. in Medicine

Data sourced from clinicaltrials.gov

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