Post-needling Soreness After Internal Gastrocnemius Muscle Treatment
Kľúčové slová
Abstrakt
Popis
Intervention:
Two zones are established:
- Zone 1: where researcher nº 1 controls the data management and sample randomization.
- Zone 2: where researcher nº 2 locates the most hyperalgesic area and measures pressure point threshold variable and researcher nº 3 performs dry needling puncture.
Researcher nº 1 explains to the subjects how the study works, collects the confidential documents and scores the independent variables (sex, age and BMI). Every subject receives an identification code and is randomly assign to a intervention group (A, B or C) Researcher nº 2 makes delivery of the document where the variables pressure pain threshold and post-needling soreness intensity will be written down. Firstly, the visual analogue scale compliance prior to the intervention is requested. After that, the subject is placed in prone position on the stretcher with a slight knee flexion and the most hyperalgesic area in the internal gastrocnemius of the lower limb with plantar fasciitis is located and marked.
Researcher nº 2 performs the algometry at the most hyperalgesic area (3 measurements with 30 seconds between them), writes down the results of pressure pain threshold variable and leaves the room.
Researcher nº 3 receives a needle from researcher nº 1 ignoring its diameter (colour tab is removed). Firstly, contamination is prevented by disinfection, then, 10 insertions are made at the marked point (the number of local twitch response are counted) and the needle used is thrown in the sanitary waste container. Ischemic compression is performed for 60 seconds followed by an analytical stretch of the internal gastrocnemius for 30 seconds.
Once researcher nº 3 has finished the intervention leaves the room and researcher nº 2 returns to repeat the measurements (post-needling soreness intensity, by filling in VAS, and pressure pain threshold, performing algometry).
Researcher nº 2 reminds the subject to complete VAS at 12, 24, 48 and 72 hours (suggesting setting an alarm) and makes an appointment 48 hours after to perform the third measure of pressure pain threshold variable.
When all the data needed for the study has been collected, researcher nº1 gathers results and exports them for statistical interpretation.
Termíny
| Naposledy overené: | 12/31/2019 |
| Prvý príspevok: | 08/13/2019 |
| Odhadovaná registrácia bola odoslaná: | 08/15/2019 |
| Prvý príspevok: | 08/18/2019 |
| Posledná aktualizácia bola odoslaná: | 01/19/2020 |
| Posledná aktualizácia bola zverejnená: | 01/21/2020 |
| Aktuálny dátum začatia štúdie: | 09/07/2019 |
| Odhadovaný dátum dokončenia primárneho okruhu: | 12/15/2019 |
| Odhadovaný dátum dokončenia štúdie: | 01/19/2020 |
Stav alebo choroba
Intervencia / liečba
Procedure: Group A treated with a 16-gauge needle
Procedure: Group B treated with a 25-gauge needle
Procedure: Group C treated with a 32-gauge needle
Fáza
Skupiny zbraní
| Arm | Intervencia / liečba |
|---|---|
| Experimental: Group A treated with a 16-gauge needle Group A is intervened on the gastrocnemius muscle with a 16-gauge needle. | Procedure: Group A treated with a 16-gauge needle We will make an application with the dry needling technique with a fine needle on the myofascial trigger points of the gastrocnemius muscle. |
| Experimental: Group B treated with a 25-gauge needle Group B is intervened on the gastrocnemius muscle with a 25-gauge needle. | Procedure: Group B treated with a 25-gauge needle We will make an application with the dry needling technique with a medium-sized needle on the myofascial trigger points of the gastrocnemius muscle. |
| Experimental: Group C treated with a 32-gauge needle Group C is intervened on the gastrocnemius muscle with a 32-gauge needle. | Procedure: Group C treated with a 32-gauge needle We will make an application with the dry needling technique with the thickest needle on the myofascial trigger points of the gastrocnemius muscle. |
Kritériá oprávnenosti
| Vek vhodný na štúdium | 18 Years To 18 Years |
| Pohlavia vhodné na štúdium | All |
| Prijíma zdravých dobrovoľníkov | Áno |
| Kritériá | Inclusion Criteria: - Age: 18-65. - Plantar Fasciitis diagnosis. - Presence of hyperalgesic area in the internal gastrocnemius. Exclusion Criteria: - Belenophobia - Hypothyroidism Presence of hyperalgesic area in the internal gastrocnemius - Diabetes - Lymphedema o lymphatic surgery Muscle diseases - Anticoagulant consumption Knee or ankle surgery - Analgesic consumption during the study |
Výsledok
Primárne výstupné opatrenia
1. Post-needling soreness intensity [Change From Baseline in Pain Scores on the Visual Analog Scale at 72 hours.]
2. Pressure Pain Threshold [Change from Baseline Pressure Pain Threshold at 72 hours]
