Burden of neck pain among medical students in Ethiopia.
Gidey Gomera Weleslassie, Hagazi Gebre Meles, Tsiwaye Gebreyesus Haile...
https://pubmed.ncbi.nlm.nih.gov/31914983/Actively Recruiting
Led by Dow University of Health Sciences · Updated on 2026-07-23
44
Participants Needed
1
Research Sites
N/A
Total Duration
This trial evaluates two treatment methods for adults aged 18 to 45 with mechanical neck pain, a common condition causing discomfort and limited neck movement without trauma or systemic disease. The study compares Transcutaneous Electrical Nerve Stimulation TENS combined with therapeutic exercises to therapeutic ultrasound combined with the same exercises. The goal is to assess their effectiveness in reducing pain and improving neck function. Participants are randomly assigned to one of two groups. One group receives TENS for 15 minutes alongside heating therapy and specific neck exercises, while the other group receives therapeutic ultrasound for 10 minutes with the same heating and exercise protocol. Both groups attend nine sessions over two weeks, with sessions lasting about 45 minutes each. During the study, participants pain intensity, muscle strength, pain threshold, and neck disability are measured before and after treatment using tools like the Visual Analog Scale and Neck Disability Index. The study also monitors functional improvements in neck movement. The total involvement period is two weeks with regular assessments to evaluate treatment effects.
CONDITIONS
TENS Versus Ultrasound With Exercise for Mechanical Neck Pain.
B
Bushra Naseem, physiotherapist
D
Dr. Saba Aijaz Ali, Physiotherapist, MSAPT
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Dow University of Health Sciences
Lead Sponsor
You may qualify if you...
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 2 weeks
Participants receive either TENS therapy or therapeutic ultrasound along with heating therapy and neck exercises. Each session lasts about 45 minutes, with a total of nine sessions over two weeks.
9 sessions over 2 weeks
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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