Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:40 AM
Ignite Modification Date:
2025-12-25 @ 1:40 AM
NCT ID:
NCT06921694
Eligibility Criteria:
Inclusion Criteria:
* Aged 18-45 years
* Participant is willing and able to give informed consent for participation in the study
* Suffering from chronic NSLBP (more than 3 months, localised below the costal margin and above the gluteal folds)
* Suffers from pain or functional limitations as a result of their LBP (minimum VAS (back) score of 3/10 or ODI score of at least 5/50 or RMD score of at least 5/24 (note, unlike ODI, RMD does not describe specific cuts offs for different levels of disability)
* Able to exercise
Exclusion Criteria:
* Radiating pain to leg / sciatica / acute radiculopathy
* Specific diagnosis/condition for LBP (e.g. herniated disk, degenerative disk disease, spondylolysis, spinal stenosis, spinal tumour, facet joint damage)
* History of osteoporosis , arthritis, scoliosis, or kyphosis.
* Current spinal infection, cancer or a current fracture (any bone).
* History of spinal/back surgery
* Unable to participate in physical activity and exercise
* Pregnant or breast feeding
* History of substance abuse
* History of psychiatric illness (eg. depression, dementia, schizophrenia) for which currently taking medication
* History or current neurological condition (e.g. epilepsy)
* Not in possession or have access to adapted equipment (phone, computer, functioning WIFI)
* Unable to understand and communicate in English
* Having taken part in a research study in the last 3 months involving invasive procedures or an inconvenience allowance
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT06921694
Study Brief:
Protocol Section:
NCT06921694