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A clinical trial to study the effect of PosturePals in Cervicothoracic Pain.

Effects of PosturePals on Pressure Pain Threshold, Cervicothoracic Muscle Activity, Craniovertebral Angle and Quality of Life among adults with Cervicothoracic Pain Syndrome: A Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079689
Enrollment
57
Registered
2025-01-29
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: M638- Disorders of muscle in diseases classified elsewhere

Interventions

Intervention1: PosturePals : Participants in the intervention group will receive PosturePals , and it will be there for 5 days/week for 4 weeks. Along with PosturePals , a standard physiotherapy proto

Sponsors

Galgotias University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Pain duration at least 6 weeks or more 2. Pain intensity score of 3 and above on NPRS at cervicothoracic region 3. Individual who has functional limitation or decreased ROM in cervicothoracic region 4. Individuals with sitting time more than 6-8 hours 5. BMI: 18.5 24.9 Kg/m2 6. Chest Circumference will be measured before the application of PosturePals 7. Participants willing to participate and provide duly signed informed consent form

Exclusion criteria

Exclusion criteria: i) History of whiplash injury, cervical and thoracic spine fracture ii) Presence of inflammatory condition such as rheumatoid arthritis, ankylosing spondylitis iii) Presence of any skin condition involving cervical and thoracic region, iv) Presence of neurological conditions such as radiculopathy, myelopathy, and epilepsy v) History of chronic pain syndrome such as fibromyalgia vi) History of psychiatric condition that might influence with study requirements vii) Tape-related allergies

Design outcomes

Primary

MeasureTime frame
1. Pressure pain threshold using algometer 2.Electromyography 3.Craniovertebral angleTimepoint: Baseline, immediately after 4-week intervention and 2-week follow-up.

Secondary

MeasureTime frame
Quality of lifeTimepoint: Baseline, immediately after 4-week intervention and 2-week follow-up.

Countries

India

Contacts

Public ContactDr Mohammad Sidiq

Galgotias University

shinny00720@gmail.com9779761606

Outcome results

None listed

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