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Study to Check and Improve Hand Strength in Phulia Handloom Weavers

ASSESSMENT AND MANAGEMENT OF HAND GRIP STRENGTH IN HANDLOOM WORKERS WITH UPPER CROSS SYNDROME - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112100
Enrollment
200
Registered
2026-06-05
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

None listed

Interventions

Intervention1: Home-Tailored Exercise Protocol for Upper Cross Syndrome (UCS).: The experimental group will follow a customized, home-based exercise protocol specifically designed to address the muscl

Sponsors

Teerthanker Mahaveer University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age: 25 40 years. Gender: Both Male and Female (unless you specify otherwise). Occupation: Active handloom workers in Phulia District with at least 1 2 years of experience. Clinical Signs: Must demonstrate postural deviations consistent with UCS (Forward Head Posture, Rounded Shoulders). Consent: Participants willing to provide informed written consent and commit to a 12-week protocol.

Exclusion criteria

Exclusion criteria: Recent Trauma: History of recent fractures or surgeries in the cervical spine, shoulder girdle, or upper limbs. Neurological Issues: Diagnosed cervical radiculopathy, disc prolapse, or peripheral nerve entrapment (e.g., Carpal Tunnel Syndrome). Systemic Conditions: Inflammatory arthritis (e.g., Rheumatoid Arthritis) or severe osteoporosis. Congenital Deformities: Any structural scoliosis or kyphosis not related to posture.

Design outcomes

Primary

MeasureTime frame
Primary Outcome Name: Hand Grip Strength. Measurement Tool: Jamar Hand Dynamometer (measured in kilograms or pounds). Secondary Outcome name: 1.Postural Alignment (Measured using REEDCO Scale) 2.Intensity of Neck and Shoulder Pain (Measured using Visual Analogue Scale) Timepoint: For Primary Outcome- Baseline (Day 0), 4 Weeks, 8 Weeks, and 12 Weeks (End of Intervention) Secondary Outcome Postural Analysis Baseline (Day 0) and 12 Weeks (End of Intervention) 2.Intensity of Neck and Shoulder Pain Baseline (Day 0), 4 Weeks, 8 Weeks, and 12 Weeks (End of Intervention)

Secondary

MeasureTime frame
Outcome 1: Postural Alignment using the REEDCO Scale. Outcome 2: Intensity of Neck/Shoulder Pain using the Visual Analogue Scale (VAS).Timepoint: Baseline and End of week 12.

Countries

India

Contacts

Public Contactkusum Agarwal

Teerthanker Mahaveer University, Moradabad

dr.naveen.s@gmail.com9634895624

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026