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3-Dimemsional release and modified active release therapy in case of mid scapular pain

comparing the efficacy of 3-Dimensional release technique and modified active release therapy on pain, scapular position and craniovertebral angle in IT workers with scapulocostal syndrome : a Randomized clinical trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059431
Enrollment
30
Registered
2023-11-02
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: 3-DIMENSIONAL RELEASE THERAPY: 3-DIMENSIONAL RELEASE THERAPY WILL BE GIVEN 3 TIMES PER WEEK FOR 2 WEEKS Duration per treatment: 45 minutes per session Control Intervention1: MODIFIED AC

Sponsors

KLE ACADEMY OF HIGHER EDUCATION AND RESEARCH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: individuals within the age group 19-40 years, presenting with medial scapular pain for more than 3 months. Pain intensity ranging from 4-8 on Numerical Pain Rating Scale. Positive Jump sign: Production of local or referred pain( in neck or forearm) on stimulation of trigger points in the medial scapular region (infraspinatus/ serratus posterior superior). Forward head posture, with CVA less than 50 degrees

Exclusion criteria

Exclusion criteria: Participants not willing to participate. history of serious systemic diseases. Spodyloarthropathies and spinal fractures. Migraine, tension-type headaches and cervicogenic headaches. Cases of degenerative shoulder joint disease. Bone fracture and/or joint dislocation, open wounds. Rotator cuff dysfunction, shoulder impingement syndrome. Pregnancy.

Design outcomes

Primary

MeasureTime frame
1. Numerical pain rating sacleTimepoint: At baseline and post 6th session—

Secondary

MeasureTime frame
Craniovertebral AngleTimepoint: Pre treatment, that is at baseline & post 6th session—

Countries

India

Contacts

Public ContactAarti Welling

KAHER INSTITUE OF PHYSIOTHERAPY

aartiwelling@klekipt.edu.in9448814569

Outcome results

None listed

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