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How to Reduce Dry Needling Pain in Treatment of Trigger Points of Muscle Triceps Sural in Ankle Post Fracture Patients

Heat or Excesice in Treadmill as Techique to Reduce Dry Needling Pain in Treatment of Trigger Points of Muscle Triceps Sural in Ankle Post Fracture Patients

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05193695
Enrollment
20
Registered
2022-01-18
Start date
2018-08-09
Completion date
2019-04-30
Last updated
2022-01-31

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

Conditions

Physical Therapy Modalities, Pain Measurement, Trigger Point Pain, Myofascial, Ankle Fractures, Rehabilitation, Needles

Keywords

Humans, Excercise therapy, Hot temperature, Post dry needling, Range of motion, articular, Muscle Strength

Brief summary

Ankle fractures are one of the main causes of hospitalization due to injuries in Chile, which also have a discharge and partial load time of approximately 12 weeks in the recovery process. This generates disuse and atrophy of the posterior musculature of the leg called the triceps sural, which makes it difficult to restart and perform the gait. We conducted this research because practically all patients with this type of diagnosis have trigger points in these muscles, and dry needling technique is one of the best for its treatment, but has the disadvantage that it produces post dry needling pain of 48 hours and there is not enough information, or consensus on which method is better to reduce post dry needling pain. This study aims to prove wich technique is most useful in reducing pain post dry needling for the treatment of trigger points in the triceps sural muscle in ankle post fracture patients.

Interventions

the patients walked on a treadmill for 20 minutes after dry needling, with an inclination of 5 degrees and at a speed at which the perceived exertion was 5 according to the Borg CR10 scale (Chen et al., 2002)

Sponsors

Becerra, Pablo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Ages between 18 and 60 years of age. * Man or woman. * At least one trigger point, active or latent, in the triceps sural muscle of the fractured ankle. * Perform full load without using technical aids.

Exclusion criteria

* Use of analgesics. * Insurmountable fear of needles. * Immune disease. * Clotting disorders. * Sensory disorders. * Psychiatric / psychological illness. * Cancer. * Rheumatic diseases.

Design outcomes

Primary

MeasureTime frameDescription
Perceived pain intensityChange from baseline (baseline and immediately after treatment)Pain will be measured by the Visual Analog Scale for pain (VAS) from 0 to 10, where higher values represent a worse outcome.
Ankle Range of Motion (ROM)Change from baseline (baseline and immediately after treatment)It is the degree of angular movement allowed by the ankle joint measured by kinovea.

Secondary

MeasureTime frameDescription
Muscular strength of triceps suralChange from baseline (baseline and immediately after treatment)By means of the heel rise test, the patient must perform a bipodal plantiflexion measured in the maximum number of repetitions in 30 seconds.

Countries

Chile

Outcome results

None listed

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