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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06437821
Other study ID # MSRSW/Batch-Fall22/717
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 1, 2023
Est. completion date October 29, 2024

Study information

Verified date May 2024
Source Superior University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This research aims to contribute valuable insights into the potential benefits of incorporating the portable wedge device into preventive or therapeutic interventions for calf-related musculoskeletal issues. By combining economical, ergonomic principles and user-friendly features, the proposed device offers individuals a convenient and efficient means to enhance their calf flexibility, ultimately mitigating strain and reducing spasms.


Description:

Developing and successfully integrating a portable wedge device could mark a significant breakthrough in preventive and rehabilitative care for musculoskeletal problems associated with the calf region. This innovative device can enhance the overall well-being and musculoskeletal health of individuals suffering from such issues, providing a more effective and convenient treatment solution.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 46
Est. completion date October 29, 2024
Est. primary completion date May 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - Male and female patients diagnosed with Trapezius tightness - Age above 18-30 - Presence of active trigger points in the upper trapezius muscle - Participants who are volunteer for the study - Patients who suffer from shoulder pain and stiffness due to bad posture Exclusion Criteria: - History of whiplash injury - History of head, neck, cervical spine or shoulder surgery - History of cervical radiculopathy - Diagnosed fibromyalgia and myopathy - History of cancer - Pregnancy Myofascial therapy within the past month - Contraindication of dry needling and instrument-assisted soft tissue mobilization technique

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Petrissage
The calf muscles will receive a firm, deep-circulation massage with fingertip pressure
Other:
Graston Technique
The calf muscles will receive a firm, deep-circulation massage with fingertip pressure

Locations

Country Name City State
Pakistan Faqraj Sharif Hospital (Trust) Physiotherapy and Orthopedic Department and Orian ABA Pakistan (Physiotherapy Department) Lahore Punjab

Sponsors (1)

Lead Sponsor Collaborator
Superior University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Numeric Pain Rating Scale (NPRS) A pain scale is a method used to quantify the level of discomfort a person is experiencing. It assesses a person's level of pain intensity on a scale from 0 to 10. The scale rates a person's level of discomfort at a particular moment and goes from '0', indicating no pain, to '10,' representing the worst pain imaginable. This simple yet efficient method is widely used to help healthcare professionals evaluate and treat pain. 12 Months
Primary Neck disability index (NDI) To evaluate a patient's functional status, ten questions are asked about their condition, including pain, personal care, lifting, reading, headaches, focus, job, driving, sleeping, and recreation. Each category is scored from 0 to 5, where 0 indicates "No pain" and 5 indicates "Worst imaginable pain." The score can be multiplied by two to get a percentage score, with a maximum score of fifty. 12 months
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