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New treatment option for Non-specific Low Back Pain
Official title Motivating Core-muscle Exercises With Wearable Sensors, Haptics and Interactive Gaming
ClinicalTrials.gov ID: NCT07555795
What this study is testing
- What it's testing
- The goal of this clinical trial is to evaluate whether a wearable biofeedback smartbelt system can improve pain and disability in adults with chronic lower back pain. The intervention combines a wearable belt that measures muscle activity with a mobile application that provides real-time feedback during exercise.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Over the age of 18
- Non-specific LBP for at least 6 weeks in the past 12 months
- Pain 4/10 on a visual analogue scale or more or Oswestry Disability Index over 20%
You likely can't join if
- Serious spinal pathology ("red flags") such as:
- History of malignancy with new onset back pain suggestive of recurrence.
- Unexplained weight loss, fever, or systemic symptoms.
- Recent significant trauma (e.g., fall from height, road traffic accident).
- Suspected or confirmed spinal infection (e.g., discitis, osteomyelitis).
- Cauda equina symptoms, including urinary retention/incontinence or saddle anaesthesia.
See the full eligibility criteria
- Over the age of 18
- Non-specific LBP for at least 6 weeks in the past 12 months
- Pain 4/10 on a visual analogue scale or more or Oswestry Disability Index over 20%
- Serious spinal pathology ("red flags") such as:
- History of malignancy with new onset back pain suggestive of recurrence.
- Unexplained weight loss, fever, or systemic symptoms.
- Recent significant trauma (e.g., fall from height, road traffic accident).
- Suspected or confirmed spinal infection (e.g., discitis, osteomyelitis).
- Cauda equina symptoms, including urinary retention/incontinence or saddle anaesthesia.
- Progressive neurological deficit (e.g., worsening weakness, loss of reflexes).
- Recent spinal surgery or invasive spinal procedures within the past 3 months.
- Severe cardiovascular or respiratory disease that prevents safe participation in mild to moderate exercise (e.g., unstable angina, uncontrolled heart failure).
- Pregnant women or those less than three months postpartum.
- Known allergy to materials used in the belt (e.g., Lycra or related fabrics).
- Cognitive impairment that prevents informed consent or ability to follow exercise instructions.
- Concurrent participation in another intervention trial that may interfere with the study outcomes.
The study team makes the final eligibility decision.
Where it's taking place
- London, United Kingdom
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include London, United Kingdom. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.