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The effect of high-frequency rTMS combined with motor control training on postural control in patients with chronic low back pain

The effect of high-frequency rTMS combined with motor control training on postural control in patients with chronic low back pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064899
Enrollment
Unknown
Registered
2022-10-21
Start date
2022-10-21
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

chronic low back pain

Interventions

Group1:motor control training

Sponsors

The First People's Hospital Affiliated to Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. The clinical diagnosis was chronic non-specific chronic low back pain, with intermittent or persistent pain between the 12th rib of the low back and the subgluteal crease for >=12 weeks; 2. Aged between 18 and 45 years; 3. Visual analogue scale (VAS) score >=3 points; 4. Open your right hand; 5. No neurological disease; 6. No drug treatment related to chronic lumbago in the past 3 months.

Exclusion criteria

Exclusion criteria: 1. Chronic low back pain due to spinal stenosis, spondylolisthesis, vertebral fracture, osteoporosis, tumor, tuberculosis, severe or progressive scoliosis, rheumatic immune/inflammatory disease (lumbar MRI should be completed for each subject with chronic low back pain); 2. Dysmenorrhea, postpartum chronic low back pain or recent/current pregnancy; 3. A history of lumbar surgery within the past 2 years, or a history of lower back or shoulder injury within the past 1 year; 4. Severe cardiovascular and cerebrovascular diseases, hypertension and blood pressure over 160/100mmHg; 5. Cancer or unexplained weight loss; 6. Mental illness; 7. Cognitive impairment, illiteracy or communication impairment; 8. Other contraindications to transcranial magnetic stimulation (metal implants in the body, previous seizure or anticonvulsant use) or other conditions that are not compatible with this study.

Design outcomes

Primary

MeasureTime frame
Pain rating scale;

Countries

China

Contacts

Public ContactWang Chuhuai

The First Affiliated Hospital, Sun Yat-sen University

Dr.Yangj@outlook.com+86 16601743624

Outcome results

None listed

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