Neck Pain Clinical Trial
Official title:
Effect of First Rib Mobilization With Balloon Breathing Exercises in Non Specific Chronic Neck Pain: A Randomized Control Trial
Verified date | August 2023 |
Source | Sehat Medical Complex |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
As Non specific chronic neck pain is effecting quality of life in many ways, there are many studies evaluating the methods to treat that problem. This study aims to determine Effect of first rib mobilization with balloon breathing exercises in non specific chronic neck pain. Patients would be divided into two groups and both received conventional treatment. Group A got conventional treatment only but Group B got 1st rib mobilization with balloon breathing exercises in addition.
Status | Completed |
Enrollment | 30 |
Est. completion date | August 24, 2023 |
Est. primary completion date | June 30, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 45 Years |
Eligibility | Inclusion Criteria: - Age group 18-45 years - Gender: Male, Female - Patients with non-specific chronic neck pain referred by physician or orthopedic surgeon - Computer users, mobile users and those with routine of prolonged sitting Exclusion Criteria: - Any H/o neurological or vestibular disorders. - Any H/o Cervical Trauma or surgery - Any history of Physiotherapy treatment for the cervical region within the previous three months - cardiac or respiratory insufficiency - Pregnancy - Neoplasm |
Country | Name | City | State |
---|---|---|---|
Pakistan | Sehat Medical Complex, Lahore | Lahore | Punjab |
Lead Sponsor | Collaborator |
---|---|
Sehat Medical Complex |
Pakistan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Neck Disability Index (change is being assessed) | Patient-completed, condition-specific functional status questionnaire with 10 items including pain, personal care, lifting, reading, headaches, concentration, work, driving, sleeping and recreation. 0-4points (0-8%) no disability, 5-14points ( 10 - 28%) mild disability, 15-24points (30-48% ) moderate disability, 25-34points (50- 64%) severe disability, 35-50points (70-100%) complete disability | Change from Baseline measures at 8 weeks | |
Primary | Numeric Pain Rating Scale (change is being assessed) | The NPRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable" | Change from Baseline measures at 8 weeks | |
Primary | Single Breath Count (change is being assessed) | Participants will be requested to count out loud after maximal inspiration. The ability to reach a count of 50 is considered as normal respiratory function | Change from Baseline measures at 8 weeks | |
Primary | Chest Wall Expansion (change is being assessed) | Take an inches tape and encircle chest around the level of nipple. Take measurements at the end of deep inspiration and expiration. Normally, a 2-5" of chest expansion can be observed |
Change from Baseline measures at 8 weeks |
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