Clinical Trials Directory

Trials / Unknown

UnknownNCT06240975

Theragun vs Dry Needling on Neck Pain, Range of Motion and Disability Among Heavy Weightlifters

Comparative Effects of Theragun and Dry Needling on Neck Pain, Range of Motion and Disability Among Heavy Weightlifters

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
28 (estimated)
Sponsor
Riphah International University · Academic / Other
Sex
Male
Age
20 Years – 35 Years
Healthy volunteers
Accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
OTHERTheragun TechniqueUse the Theragun for a designated duration per session, such as 5-10 minutes for one session per week for 6 weeks
OTHERDry Needling TechniqueDry needle deep (20 mm) TrP acupuncture of myofascial duration per session, such as 5-10 minutes for one session per week for 6 weeks

Timeline

Start date
2023-10-20
Primary completion
2024-02-20
Completion
2024-02-20
First posted
2024-02-05
Last updated
2024-02-05

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT06240975. Inclusion in this directory is not an endorsement.