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Microwave Diathermy for Treating Nonspecific Chronic Neck Pain

Microwave Diathermy for Treating Nonspecific Chronic Neck Pain. A Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01487122
Acronym
MOFIS
Enrollment
145
Registered
2011-12-07
Start date
2008-09-30
Completion date
2011-09-30
Last updated
2011-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain

Keywords

Diathermy, Neck Pain

Brief summary

This randomised controlled trial aims to compare the effect of microwave diathermy (continuous and pulsed modes) with sham microwave diathermy in nonspecific chronic neck pain patients. Every patient will also be treated by exercise and transcutaneous electrical neurostimulation (TENS). The primary endpoint is to establish whether the use of microwaves is justified in terms of pain relief or reduction of disability in this patients.

Interventions

RADIATIONContinuous microwave

Continuous microwave through a great circular electrode, 15 cm from the neck, 20 minutes, 80 watts, 15 sessions in 3 weeks

RADIATIONPulsed microwaves

Pulsed microwaves through a great circular electrode, 15 cm away from the neck, 20 minutes, 80 watts, 15 sessions in 3 weeks

PROCEDURESham microwaves

Unplugged microwave generator, great circular electrode, 15 cm away from the neck, 20 minutes, 15 sessions in 3 weeks

Sponsors

Health Service of Andalucia
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* to be between 18 and 65 years old * to be diagnosed with chronic nonspecific neck pain (i.e. during more than 3 months in the absence of red flags (unexplained weight loss, fever, neurological signs, history of cancer, history of inflammatory conditions...)

Exclusion criteria

* pregnancy * sick leave * litigation * claims because the neck pain.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in pain at six monthsBaseline. At three weeks. At six monthsPain as measured by visual analogic scale
Change from baseline in neck disability at six monthsBaseline. At three weeks. At six monthsNeck disability as measured by Neck Disability Index and Northwick Park Neck Pain Questionnaire
Change from baseline in quality of life at six monthsBaseline. At three weeks. At six monthsQuality of life as measured by SF-36 questionnaire

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026