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Study on Neck Muscle Activity and Fatigue During Theraband Exercises in People with Chronic Neck Pain

Analysis of Cervical Muscle Activity and Fatigue in Response to Moderate Intensity Theraband Exercises in Patients with Persistent Neck Pain - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090776
Enrollment
48
Registered
2025-07-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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: Moderate Intensity TheraBand training: Participants in the intervention group will perform a structured, moderate-intensity Theraband exercise protocol targeting both deep and superfici

Sponsors

Galgotias University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Individuals diagnosed with persistent non-specific Neck Pain for more than 3 months duration. Neck Disability Index score indicating mild to moderate disability Able to perform basic neck movements without severe restriction. Willingness to participate and provide informed written consent.Able to understand and follow instructions for exercise protocol and assessments.

Exclusion criteria

Exclusion criteria: History of neck surgery or trauma in the past 6 months. Specific neck pathology (e.g., cervical radiculopathy, myelopathy, disc herniation, inflammatory arthritis, tumor). Neurological disorders affecting muscle function (e.g., stroke, multiple sclerosis, Parkinson s disease). Pregnancy, due to potential risk during exercise. Current physiotherapy treatment for neck pain or recent participation in a neck strengthening program (within last 3 months). Use of muscle relaxants or corticosteroids during the study period. Systemic illnesses such as uncontrolled diabetes, hypertension, or thyroid disorders affecting fatigue or musculoskeletal function.Cognitive impairments or psychiatric conditions that hinder understanding of instructions or participation.

Design outcomes

Primary

MeasureTime frame
Surface EMG Muscle Activity Pressure pain threshold NPRS for painTimepoint: At Baseline, 8 weeks after 26 weeks

Secondary

MeasureTime frame
Fatigue Severity ScaleTimepoint: At Baseline, 8 weeks after 26 weeks

Countries

India

Contacts

Public ContactDr Jyoti Sharma

GALGOTIAS UNIVERSITY

sidufatima@gmail.com06006204628

Outcome results

None listed

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