Primary headache
Conditions
Interventions
interview - High-benefit group:Semi-structured interview
interview - Low-benefit group:Semi-structured interview
interview - Dropout group:Semi-structured interview
Genetic factors - High-benefit group:Single Nucleotide Polymorphisms Analysis
Genetic factors - Low-benefit group:Single Nucleotide Polymorphisms Analysis
Sponsors
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: 1. Clinical data mining section (1) Participated in the "Case Registration Study on the Treatment of Chronic Primary Headaches with Five-Element Acupuncture" conducted by our research group (Project Number: CI2021A03510); (2) Upon verification, the treatment was completed strictly following the preliminary research protocol, and there were no missing data for the primary efficacy indicators; (3) No restrictions on age or gender; Those who meet all three criteria above will be included. 2. Value and preference section (1) Participated in the "Case Registration Study on the Treatment of Chronic Primary Headaches with Five-Element Acupuncture" conducted by our research group (Project Number: CI2021A03510); (2) Have the ability to understand the explanation of this study and voluntarily make a decision on whether to participate; (3) Aged=18 years, of either gender; (4) Voluntarily sign the informed consent form. Those who meet all four criteria above are eligible to participate in this interview. 3. Genetic factors (1) Participated in the "Case Registration Study on the Treatment of Chronic Primary Headaches with Five-Element Acupuncture" conducted by our research group (Project Number: CI2021A03510); (2) Strictly follow the preliminary research protocol to complete the treatment, with no missing data for the primary efficacy indicators; (3) Aged=18 years, of either gender; (4) No new major neurological diseases (such as stroke, epilepsy) have occurred within the past year; (5) Agree to provide a saliva sample; (6) Voluntarily sign the informed consent form. Those who meet all the above six criteria will be included.
Exclusion criteria
Exclusion criteria: 1. Clinical data mining section This analysis will be strictly based on the per-protocol set from the previous study (CI2021A03510). Informed consent waiver has been applied. Therefore, no additional exclusion criteria will be set for this part. 2. Value and preference section (1) Individuals with severe auditory, language, or cognitive impairments are unable to communicate effectively; (2) The researcher determines that the individual's current mental or cognitive state is not suitable for participating in the interview (such as the presence of acute psychiatric symptoms, cognitive impairment, etc.); (3) The researcher judges that the individual currently suffers from severe and unstable physical illnesses, and participating in the interview may be detrimental to their health; (4) The researcher judges that any other situational factors may prevent them from completing the interview or render the data invalid. Anyone who meets one of the criteria will be excluded. 3. Genetic factors (1) Special physiological conditions, such as women in pregnancy or those who have been preparing for pregnancy in the past three months; (2) Have used immunosuppressants in the past three months or undergone major surgery or trauma in the past six months; (3) Participating in other clinical research studies. Anyone who meets one of the criteria will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical characteristics of different beneficiary population;Value and preference characteristics of different beneficiary population;Genetic characteristics of different beneficiary population; | — |
Countries
China
Contacts
Public ContactWang Jing-jing
Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences
Outcome results
None listed