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The Effects of Balanced Seating Pressure on Pelvic Asymmetry in Under-Buttocks Pressure, Spinal Alignment, and Lower Back Pain: A Pilot Study

Status: Recruiting
Location: See location...
Intervention Type: Device, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to learn if the DaSuit® cushion helps reduce discomfort caused by sitting in adults with non-specific low back pain. It will also assess the safety and physical effects of using the DaSuit® cushion. The main questions it aims to answer are: 1. Does the DaSuit® cushion distribute the pressure evenly on both under-buttock pressure compared to a placebo cushion? 2. Does the DaSuit® cushion improve spinal alignment compared to a placebo cushion? 3. What discomfort or adverse events do participants experience when using the DaSuit® cushion? Researchers will compare the DaSuit® cushion to a placebo cushion (a look-alike cushion without therapeutic effect) to see if the DaSuit® cushion works to relieve sitting-induced discomfort. Participants will: 1. Use the DaSuit® cushion or a placebo cushion in a randomized order, with each sitting session lasting 10 minutes 2. Complete both conditions with a 10-minute washout period between sessions 3. Sit on a standardized wooden chair with a pressure sensor mat placed on the cushion surface 4. Keep a fixed posture with hips, knees, and ankles at approximately 90 degrees 5. Watch a 10-minute video on a tablet positioned 30-40 cm in front of them at a 5-10 degree downward angle to maintain a steady gaze 6. Undergo spinal imaging immediately after each session, maintaining the same seated posture 7. Report any discomfort or pain experienced during or after each session

Eligibility
Participation Requirements
Sex: All
Minimum Age: 20
Maximum Age: 50
Healthy Volunteers: f
View:

• adults aged 20 to 50 years

• adults had low back pain non-specific but exacerbated by sitting with VAS score between 3-7

• body height between 150-180 cm

• BMI between 18.5-24

• a radiographically verified hemi-pelvic height discrepancy of ≥ 0.3 cm in sitting posture

• willing to participate and cooperate throughout the whole intervention session

Locations
Other Locations
Taiwan
Taoyuan Chang Gung Memorial Hospital
RECRUITING
Taoyuan District
Contact Information
Primary
Wei-Han Chang, M.D., PhD.
weihan7252@gmail.com
+886 975365711
Backup
Hander Wang, M.D.
superr401@gmail.com
+886 975366879
Time Frame
Start Date: 2025-09-12
Estimated Completion Date: 2026-05-15
Participants
Target number of participants: 20
Treatments
Other: Dasuit to Placebo
This group of patients will first undergo Dasuit intervention then Placebo intervention
Other: Placebo to Dasuit
This group of patients will first undergo Placebo intervention then Dasuit intervention
Related Therapeutic Areas
Sponsors
Leads: Chang Gung Memorial Hospital

This content was sourced from clinicaltrials.gov