The study is randomized and single-blinded. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A \& B through sealed envelope method by Non-probability Convenient random sampling technique. Subjects in Group A will receive Theragun technique. Group B will receive Dry Needling technique.
The objective of the study is to determine the Comparative effects of theragun and dry needling on neck pain, range of motion and disability among heavy weightlifters. The study is randomized and single-blinded. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A \& B through sealed envelope method by Non-probability Convenient random sampling technique. Subjects in Group A will receive Theragun technique. Group B will receive Dry Needling technique. Neck Disability index (NDI), Universal Goniometer, Numeric Pain Rating Scale (NPRS) will be used to assess at the baseline and after the completion of treatment at 6 weeks. The data will be analyzed by SPSS, version 25. Statistical significance is P=0.05.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Enrollment
28
Use the Theragun for a designated duration per session, such as 5-10 minutes for one session per week for 6 weeks
Dry needle deep (20 mm) TrP acupuncture of myofascial duration per session, such as 5-10 minutes for one session per week for 6 weeks
Pakistan sports board
Lahore, Punjab Province, Pakistan
RECRUITINGDisability
The Neck Disability Index (NDI) is commonly used for clinical and research assessment for chronic neck pain
Time frame: pre and 6 weeks post interventional
Range of Motion
A goniometer is an instrument that measures the available range of motion at a joint
Time frame: pre and 6 weeks post interventional
Neck Pain
Patient level of pain will be assessed using this Numerical Pain Rating Scale (NPRS)
Time frame: pre and 6 weeks post interventional
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