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Efficacy of Proprioceptive Neuromuscular Facilitation in Pain Relief

Efficacy of Proprioceptive Neuromuscular Facilitation in Pain Relief in Women With Migraine

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02549885
Acronym
PNF
Enrollment
30
Registered
2015-09-15
Start date
2016-04-30
Completion date
2017-08-31
Last updated
2018-03-15

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

Conditions

Migraine Disorders

Keywords

Migraine disorders, Muscle stretching exercises

Brief summary

The purpose of this study is to determine whether the contract-relax technique of proprioceptive neuromuscular facilitation, and the static stretching exercise are effective in reducing the frequency, intensity and duration of headache and in improving the perception of quality of life in women with migraine.

Detailed description

This is an randomized clinical trial, double blind, comparing two interventions in women with migraine, whose diagnosis was confirmed by a neurologist.

Interventions

OTHERPNF contract-relax

Proprioceptive neuromuscular facilitation, using the technique of contract-relax on neck diagonal.

OTHERStatic stretching

Static stretching of neck muscles.

Sponsors

Universidade Federal de Pernambuco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Age between 18and 40 years * Clinical diagnosis of migraine * Participants with at least one day with acute migraine per month, with attacks lasting 4-72 hours.

Exclusion criteria

* Obesity type I, II or III, according to the classification of Body Mass Index. * Pregnancy, lactation or both. * Presence of meningitis, demyelinating diseases, cerebral aneurysm, intracranial hypertension, myopathies, myelopathy, fibromyalgia, symptomatic neck disc herniation, rheumatoid arthritis and history of tumors in the brain or spine. * Participants who performed other manual therapeutic interventions or other physical therapy modalities in the head or neck during the survey period. * Participants who have daily prophylactic medication for migraine.

Design outcomes

Primary

MeasureTime frameDescription
Pain changeChange from Baseline Pain at 8th - 10th week; Change from Baseline Pain at 12th - 14th weekDaily headache
The global perception of changeglobal perception of change at 12th - 14th weekPatient Global Impression of Change Scale
Feasibility for successful random allocation12 monthssuccessful random allocation of 30 patients during a 12-months period
Proportion of eligible patients randomly assigned for each group (target ≥70%)12 monthsthe proportion of eligible patients randomly assigned for each group (target ≥70%)
Proportion of eligible patients who completed 30-day follow-up (target ≥95%)12 monthsthe proportion of randomly assigned patients who completed 30-day follow-up after the end of the treatment (target ≥95%)

Secondary

MeasureTime frameDescription
Change in Medicine intake in migraine attacksChange from Baseline Medicine intake at 8th - 10th week; Change from Baseline Medicine intake at 12th - 14th weekDaily headache
Change in severity of migraine-related disabilityChange from Baseline Migraine disability assessment at 8th - 10th week; Change from Baseline Migraine disability assessment at 12th - 14th weekQuestionnaire Migraine disability assessment
Change in Adverse effects of the interventionChange from Baseline adverse effects at 8th - 10th week; Change from Baseline adverse effects at 12th - 14th weekDaily headache
Change in Neck mobilityChange from Baseline neck mobility at 8th - 10th week; Change from Baseline neck mobility at 12th - 14th weekGoniometer Cervical Range of Motion (CROM)
Change in pressure pain thresholdChange from Baseline pressure pain threshold at 8th - 10th week; Change from Baseline pressure pain threshold at 12th - 14th weekComputerized Algometer
Change in neck disability indexChange from Baseline neck disability index at 8th - 10th week; Change from Baseline neck disability index at 12th - 14th weekQuestionnaire Neck disability index

Countries

Brazil

Outcome results

None listed

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