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A Multi-center Clinical Longitudinal Study of Neuropathic Pain by Collecting Data

A Multi-center Clinical Longitudinal Study of Neuropathic Pain by Collecting Data on Patients' Brain Physiology and Cognitive Function

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06290024
Enrollment
2000
Registered
2024-03-04
Start date
2023-08-15
Completion date
2025-07-15
Last updated
2024-11-13

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

Conditions

Pain

Brief summary

A multi-center clinical longitudinal study of neuropathic pain by collecting data on patients' brain physiology and cognitive function

Detailed description

Using the use of pain visual analog scale (VAS), digital pain grading method (NRS), neuropathic pain assessment scale (DN4), sleep quality (Pittsburgh sleep quality index, Ascens insomnia scale), social support assessment scale (SSQ), Montreal cognitive assessment scale (MoCA), Barrett impulse scale (BIS), anxiety and depression score (GAD-7, PHQ-9), emotional tasks, cognitive function (N-back, time perception, delay-discount), electroencephalogram (EEG), near-infrared brain function imaging (fNIRS) and other indicators to study the dynamic changes of various factors in the process of acute pain.

Interventions

DEVICEA multi-center clinical longitudinal study of neuropathic pain by collecting data on patients' brain physiology and cognitive function

Using the use of pain visual analog scale (VAS), digital pain grading method (NRS), neuropathic pain assessment scale (DN4), sleep quality (Pittsburgh sleep quality index, Ascens insomnia scale), social support assessment scale (SSQ), Montreal cognitive assessment scale (MoCA), Barrett impulse scale (BIS), anxiety and depression score (GAD-7, PHQ-9), emotional tasks, cognitive function (N-back, time perception, delay-discount), electroencephalogram (EEG), near-infrared brain function imaging (fNIRS) and other indicators to study the dynamic changes of various factors in the process of acute pain.

Sponsors

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. The subjects voluntarily participated in the study and signed an informed consent form; 2. The age is between 18 years old (inclusive) and 85 years old (inclusive), regardless of gender; 3. Body mass index (BMI) ≤ 45; 4. Clinically clearly diagnosed neuropathological pain (pain VAS score ≥4 or above); 5. Did not participate in the drug/medical device test within 3 months before the test;

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
(Patient Health Questionnaire-91 monthCalculate the total score 0-4 points: no depression (take care of yourself) 5-9: possible mild depression (consult a psychologist or medical worker recommended) 10-14 points: There may be moderate depression (preferably consult a psychologist or psychological medicine worker) 15-19: possible moderate to severe depression (consult a psychiatrist or psychiatrist) 20-27: possible severe depression (be sure to see a psychologist or psychiatrist) Core project points Item 1, item 4, item 9, any question score\> 1 (select 2,3), need attention; item 1, item 4, representing the core symptoms of depression; Item 9 represents a self-injury mind.
Barrett impulse scale (BIS)1 monthThe subject's feeling, reaction and degree of recognition are regarded as evaluation indicators, and the five-point scale classification method is adopted. Action impulse is scored positively, and unplanned impulse and cognitive impulse are scored in reverse. The standard is: 1 means never or almost never; 2 means occasional; 3 means often; 4 means always or almost always.
(Generalized Anxiety Disorder,GAD-7)1 monthEach entry is 0 to 3 points, the total score is the score of the 7 items, the total score ranges from 0 to 21 points A 0-4 score is found without a GAD And 5-9 points for mild GAD And 10 - 14 points for moderate GAD 15 - 21 for severe GAD
Visual Analogue Scale/Score(VAS)1 monthVAS pain score criteria ((0-10 points) 0 Points: painless; 3 points below: have a slight pain, can tolerate; 4 points- -6 points: patients with pain and affect sleep, and can still tolerate; 7 points-10 points: the patient has gradually intense pain, the pain is unbearable, affect appetite, affect sleep.
digital pain grading method (NRS)1 monthScore ranged from 1 to 5, and the higher the score, the more it suggested the possibility of neuropathic pain. Clinically, when patients score ID Pain 3, neuropathic pain-related treatment options will be considered.
neuropathic pain assessment scale (DN4)1 monthEach assessment item was assigned 1 point for yes and 0 point for no. The total score of DN4 is 0 to 10, and neuropathic pain when the total score is greater than or equal to 4.
sleep quality (Pittsburgh sleep quality index, Ascens insomnia scale)1 monthThe PSQI was used to assess the sleep quality of the participants in the last 1 month. It consists of 19 self-assessment entries and 5 items, among which the 19th self-assessment entry and 5 items do not participate in the scoring. Only the 18 self-assessment entries participating in the scoring are introduced here (see the attached questionnaire for details). The 18 items formed 7 components, and each component was scored according to 0-3 levels. The cumulative score of PSQI total score ranged from 0 to 2 l. The higher the score, the worse the sleep quality.
EEG1 monthTo study the dynamic change of EEG wavelength during the progression from acute pain to chronic pain,four basic waveforms, α, β, θ, δ wave, were collected。

Secondary

MeasureTime frameDescription
ocial support assessment scale (SSQ)1 monthEach group of questions asked (A) how satisfied you are with the number of people who help or support you in your life, and (B) how satisfied you are with the way they / they help you.1= very dissatisfied, and 6= very satisfied.
Montreal cognitive assessment scale (MoCA)1 monthThe Montreal Cognitive Assessment (Montreal Cognitive Assessment, MoCA) is a rating tool for rapid screening of cognitive abnormalities. It includes eight cognitive domains, including visual structure skills, executive function, memory, language, attention and concentration, calculation, abstract thinking and directional force. The total score of 30 and 26 were normal, with high sensitivity, covering important cognitive fields, short test time and suitable for clinical use.

Countries

China

Contacts

Primary Contactjingting chen, phd
806041409@qq.com13122778387
Backup Contactke ma, phd
marke72@163.com13361879260

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026