Skip to content

Clinical trial on back pain & shoulder pain patients

A Prospective, open label study to assess the Posture Corrector belt for correcting the posture in both Male & female volunteers with back pain and shoulder pain.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/053282
Enrollment
15
Registered
2023-05-31
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Health Condition 1: M500- Cervical disc disorder with myelopathy

Interventions

Intervention1: Posture Corrector: if a person is a beginner, start by wearing it for 30 mins a day, 3-4 times a week, gradually increasing it to every day. The maximum you can extend it to 2-3 hours a

Sponsors

UNITED MEDICARE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Indian volunteers aged between 18-70 years. 2. Willing to give Informed Consent Form. 3. Willing to complete the study assessments/questionnaires. 4. Subjects having moderate back and shoulder pain with altered posture. 5. Subjects suffering from muscle spasm, strained muscles/ligaments, 6. muscle tension, damaged disks, injuries, or falls, arthritis, osteoporosis, unusual curve of spine, and disk bulging.

Exclusion criteria

Exclusion criteria: 1. Pregnancy or breast feeding 2. Evidence of active concomitants pulmonary disease other than asthma. 3. Chronic illness or had major surgery in the last 1 year. 4. Concomitant severe decompensated systemic disease (cardiovascular, renal, hepatic, endocrine, hematological, neurological, immunological) 5. Patients with pre-existing severe systemic disease necessitating long-term medication. 6. History of cancer, including solid tumors, hematologic malignancies and carcinoma in situ. 7. Any neurological (congenital or acquired), vascular or systemic disorder which could affect any of the efficacy assessments. 8. Participation in the current or previous clinical trial with any approved or investigational products during the past 1 month.

Design outcomes

Primary

MeasureTime frame
1.Percentage improvement in Degree of thoracic kyphosis & lumbar lordosis assessed by flexi ruler & visual assessments to determine the improvement of posture of the subjects. 2.Percentage Improvement in pain reduction in subjects suffering from muscle spasm, strained muscles/ligaments, muscle tension, damaged disks, injuries, or falls, arthritis, osteoporosis, unusual curve of spine, and disk bulging through the Quebac Back Pain Disability Scale Timepoint: Day 0 Day 15 & Day 30

Secondary

MeasureTime frame
Consumer acceptance for effective support to pull muscles & spine back to original alignment and relief from the pain will be assessed through feedback questionnairesTimepoint: Day 0 to Day 30

Countries

India

Contacts

Public ContactDr Ashok Godavarthi

Radiant Research Services Pvt. Ltd

surya.ashok@gmail.com9880999297

Outcome results

None listed

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