Can magnetic pulses help restore swallowing?
NCT ID NCT07765043
First seen Aug 14, 2026 · Last updated Aug 19, 2026 · Updated 2 times
Summary
This study tests whether pulsed electromagnetic field therapy (PEMT) can improve swallowing function in people with cervicogenic dysphagia, a swallowing disorder caused by neck problems. Forty adults aged 50-60 with this condition will receive either real or placebo PEMT, along with swallowing exercises, twice a week for eight weeks. Researchers will measure changes in swallowing difficulty and the impact of dysphagia on daily life to see if the magnetic therapy adds benefit beyond exercise alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pulsed electromagnetic field therapy (PEMT) combined with swallowing resistance training exercises
- What this could lead to
- If effective, this could offer a non-invasive, drug-free way to improve swallowing and reduce the handicap of cervicogenic dysphagia.
- What could go wrong
- This is a small early-stage trial with only 40 participants, so results may not apply broadly. The placebo effect and the added exercise program could also influence outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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40 people
The number who actually took part.
- Started
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Jul 2025
- Finished
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May 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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50 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Individuals diagnosed with cervicogenic dysphagia and cervical spondylosis * Age 50-60 years. * Individuals with a sedentary lifestyle (less than 30 minutes of aerobic activities per day). * Signed the written consent Exclusion Criteria: * Subjects diagnosed with rheumatological disease, cerebrovascular abnormalities * Subjects having a metal implant or previous cervical surgeries. * Subjects having received physical therapy programs for cervical spondylosis or dysphagia within the last 6 months. Subjects with recent infection, cognitive impairments or dementia, cardiovascular instability, head or neck traumatic injuries, neurological disorders affecting swallowing (e.g., parkinsonism, stroke). * Subjects who received medications interfering with normal swallowing function (e.g., antiepileptics, antipsychotics, and antidepressant drugs). * Subjects who refused to provide the signed informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Umm Al-Qura University
Mecca, 24351, Saudi Arabia
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