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Concomitant or sole treatment of Chuna manual therapy and pharmacopuncture on Neck & Back pain in patients with Traffic Injuries : A preliminary, prospective, observational registry study

Not Applicable
Completed
Conditions
Diseases of the musculo-skeletal system and connective tissue
Registration Number
KCT0002712
Lead Sponsor
Pusan National University Korean Medicine Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
120
Inclusion Criteria

1. Neck pain or Low back pain patients with traffic injuries which applied to Whiplash Associated Disorders (WAD) grade I, II
2. Patients with average Numeric Rating Scale (NRS) =5
3. Patients who need to be treated with Chuna manual therapy or pharmacopuncture treatment or concomitant treatment of both depending on practitioner's decision
4. Patients aged 19 years or older and 70 years or younger
5. Patients who can communicate normally
6. Patients who have agreed to trial participation and provided written informed consent

Exclusion Criteria

1. Low back pain or neck pain patients which were caused by other causes except for traffic accident. (e.g osteoarthritis, rheumatoid arthritis, fibromyalgia syndrome, gout etc)
2. Patients with a chronic illness that may affect clinical outcomes.
3. Patients who had undergone cervical, lumbar spine surgery previously.
4. Patients with congenital spinal disorder
5. Patients who have participated in other clinical studies within the past month.
6. Patients who can not communicate normally due to dementia or mild cognitive impairment.
7. Pregnant woman
8. Patients who can not perform clinical research normally according to judgment of researcher

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
umeric Rating Scale (NRS)
Secondary Outcome Measures
NameTimeMethod
Disability Index [Oswestry Disability Index (ODI) /Neck Disability Index (NDI)];EuroQol-5 Dimension (EQ-5D) ;Satisfaction (9-point Likert scale);Adverse events
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