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Effect of Kinesio tape on chronic low back pain: a prospective randomized controlled and multi-center trial

Effect of Kinesio tape on chronic low back pain: a prospective randomized controlled and multi-center trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016168
Enrollment
Unknown
Registered
2018-05-16
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

low back pain

Interventions

KT therapy group:KT therapy
Comprehensive therapy group:KT + exercise therapy

Sponsors

Shanghai University of Sport
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. 18–60 years old 2. With a diagnosis of CLBP symptoms 3. Symptoms that last for more than 3 months 4. Lack of abnormal sense and reflection of the lower extremity 5. Medication not expected to change during the study period 6. Availability of three times a week over a period of 3 months

Exclusion criteria

Exclusion criteria: 1. Undergone previous surgery, dislocation, fracture, rheumatoid arthritis, and ankylosing spondylitis 2. Severe cardiovascular, progressive neurological deficits, severe osteoporosis, or metabolic diseases 3. Low back pain caused by visceral disease 4. VAS score (from 1 to 10) above 8 5. Inability to communicate in Chinese 6. Attended exercise therapy or used KT during the last 3 months 7. Pregnant or lactating 8. Uncontrolled hypertension 9. Other illness, judged by the patient or study physician, to make participation in this study inadvisable.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale (VAS) score;back function;muscle strength of spine;proprioception;

Secondary

MeasureTime frame
SF-36;muscle morphology: musculoskeletal ultrasound;

Countries

China

Contacts

Public ContactXueqiang Wang

Shanghai University of Sport

qiang897@163.com+86 18601612741

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026