Immediate Effect of Acupuncture Versus Electroacupuncture on Explosive Force Production of Quadriceps Muscle in Healthy Subjects
NCT ID: NCT07037342
Last Updated: 2025-06-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
66 participants
INTERVENTIONAL
2024-04-15
2025-05-25
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Echo-guided Percutaneous Electrical Nerve Stimulation of the Femoral Nerve
NCT06894537
Efficacy of of Acupuncture Laser Therapy on Hemodialysis Patients
NCT07099352
Acupuncture Versus Transcutaneous Electrical Nerve Stimulation on Pain Post Upper Abdominal Surgeries
NCT07036393
Acute Effects of Transcutaneous Electrical Nerve Stimulation at Acupoints on Nociceptive Transmission: A Mechanism Study Using Pain-Related Evoked Potentials
NCT07267052
Comparison of the Analgesic Effects of Acupuncture and Modulated Electroanalgesia in Cold Induced Pain
NCT01483885
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Manual acupuncture
22 patients will receive manual acupuncture on acupoint for 20 minutes
Manual acupuncture
Manual acupuncture on acupoint (ST32, ST34, ST36, SP10) the needles will be inserted perpendicularly for 20 minutes.
Electro acupuncture
22 patients will receive electro acupuncture on acupoint for 20 minutes
Electro acupuncture
Electro acupuncture on acupoint (ST32, ST34, ST36, and SP10) for 20 minutes.
Sham acupuncture
22 subjects will receive sham acupuncture for 20 minutes
Sham acupuncture
Is a needle insertion at wrong points or non-points (locations that are not known acupuncture points)
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Manual acupuncture
Manual acupuncture on acupoint (ST32, ST34, ST36, SP10) the needles will be inserted perpendicularly for 20 minutes.
Electro acupuncture
Electro acupuncture on acupoint (ST32, ST34, ST36, and SP10) for 20 minutes.
Sham acupuncture
Is a needle insertion at wrong points or non-points (locations that are not known acupuncture points)
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Right leg dominant .
* Age between 18 to 23.
* Body mass index ˂ 25 kg/m\^2.
* Normal daily life activities.
Exclusion Criteria
* Under supervision of other heath practitioner.
* Involved in regular strength training during 6 months prior to the study.
* Impaired sensation or any neurological/ musculoskeletal disorder.
* Pregnant females.
18 Years
28 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Egyptian Chinese University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Rowan Mohamed Raga
principle investigator : rowan mohamed raga
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Egyptian Chinese University
Cairo, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
P.T.RCT/012/004967
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.