Evaluation of the Kinesiology Taping Effectiveness in the Treatment of Lumbar Spine Pain
Evaluation of the Kinesiology Taping Effectiveness in the Treatment of Lumbar Spine Pain in Subjects Under 30 Years of Age
Lumbar spine pain syndromes are one of the most common pain conditions in our society.
The purpose of kinesiotaping is to normalize muscle function, improve blood and lymph flow, reduce pain, improve proprioception, promote tissue healing and restore normal tissue function. Today, this method is used in many fields of medicine. Its primary purpose is to support the musculoskeletal system by using various types of applications.
There is a lack of publications in the global literature on the effect of kinesiotaping of the external oblique muscles on lumbar spine pain. The main objective of this study is to evaluate the effectiveness of kinesiology taping in the treatment of lumbar spine pain in individuals under 30 years of age.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Back pain occurs in people of all ages, regardless of their job. Both blue-collar and white-collar workers are exposed to strain and pain in the lumbar spine. The presence of pain is also promoted by low physical activity, poor motor habits, as well as stress.
There are numerous factors affecting the quality of life in patients with lower back pain. These include degree of pain, physical fitness, individual factors, degree of social support, and a potential for adapting forces to match constantly changing conditions.
The contemporary functional model of lumbar spinal muscles divides them into local stabilizers, single-joint global stabilizers, and multi-joint global stabilizers. The abdominal external oblique muscles are classified as global stabilizers. They generate force to control range of motion and allow limitation of that range (eccentric control), and functionally control rotation in all movements, regardless of the load acting on the spine.
The main objective of this study is to evaluate the effectiveness of kinesiology taping in the treatment of lumbar spine pain in individuals under 30 years of age.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
-
-
-
Biała Podlaska, Pologne, 21-500
- Pope John Paul II State School Of Higher Education in Biała Podlaska
-
Biała Podlaska, Pologne
- Laboratory of Pope John Paul II State School Of Higher Education in Biala Podlaska
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- participants' age between 18 and 30,
- the presence of pain in the lumbar region of the spine,
- participants who have not been using non-steroidal anti-inflammatory drugs (NSAIDs) for at least one week prior to study entry,
- no contraindications to the use of dynamic kinesiology taping patches,
- informed, written consent to participate in the study.
Exclusion Criteria:
- status of the post lumbar spine surgery,
- subjects who have had a spinal injury within 6 months prior to the start of the study,
- neoplastic diseases,
- congenital structural pathologies of the spine,
- allergy to the adhesive substance of kinesiology taping or paper patch,
- being a physiotherapy student.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Tripler
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Dynamic tape
Experimental group will use a special dynamic tape on the lumbar extensor muscles
|
The experimental group will use a special dynamic patch made of cotton, coated with a hypoallergenic acrylic heat-activated adhesive arranged in sinusoidal-shaped layers.
The tape will be applied using the muscle technique with a Y-shaped cut patch directly to the dried and non-greased skin.
The application will be performed in a standing position, with the participant's lower extremities straight.
The therapist will place the beginning of the tape (the base) on the participant's sacrum and then, asking them to bend 45 degrees forward, tape the tails of the tape along the spine on the extensor muscles of the lumbar region, without changing the tension of the tape, keeping the base in the initial position.
|
|
Comparateur factice: Paper tape
Control group will use a paper tape on the lumbar extensor muscles
|
In the control group, a plain paper patch will be used to conduct the study, which, like the dynamic patch, will be applied using the same form of tape cutting and the same application technique.
The entire method of applying the patch will also take place in the participant's standing position with forward bending.
The paper patch will be placed at the levels from the L3 segment to the sacrum, along the spine on the lumbar extensor muscles.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Visual analogue scale of pain (VAS)
Délai: Visual analogue pain scale (VAS) will be carried out before the start of the therapy.
|
Visual analogue scale of pain (VAS) evaluates intensity of pain in the scale from 0 to 10. Maximum score means the highest level of pain.
|
Visual analogue pain scale (VAS) will be carried out before the start of the therapy.
|
|
Visual analogue scale of pain (VAS)
Délai: Visual analogue pain scale (VAS) will be carried out 4 days of therapy, immediately after its completion.
|
Visual analogue scale of pain (VAS) evaluates intensity of pain in the scale from 0 to 10. Maximum score means the highest level of pain.
|
Visual analogue pain scale (VAS) will be carried out 4 days of therapy, immediately after its completion.
|
|
Visual analogue scale of pain (VAS)
Délai: Visual analogue pain scale (VAS) will be carried out four weeks after the end of the treatment.
|
Visual analogue scale of pain (VAS) evaluates intensity of pain in the scale from 0 to 10. Maximum score means the highest level of pain.
|
Visual analogue pain scale (VAS) will be carried out four weeks after the end of the treatment.
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Modified Laitinen's pain questionnaire
Délai: Modified Laitinen's pain questionnaire will be carried out three times (before the start of the therapy, after 4 days of therapy, immediately after its completion and four weeks after the end of the treatment
|
The Laitinen questionnaire takes into account four indicators evaluated in a scale of 0 to 4: the intensity of pain, the frequency of its occurrence, the use of analgesic medications and limitation of the participant's motor activity.
A research participant could be granted from 0 to 16 points, the maximum score meaning the highest level of pain.
|
Modified Laitinen's pain questionnaire will be carried out three times (before the start of the therapy, after 4 days of therapy, immediately after its completion and four weeks after the end of the treatment
|
|
Oswestry Disability Index
Délai: Oswestry Disability Index will be carried out three times (before the start of the therapy, after 4 days of therapy, immediately after its completion and four weeks after the end of the treatment
|
Oswestry Disability Index takes into account ten indicators evaluated in a scale of 0 to 5. A research participant could be granted from 0 to 50 points, the minimum score meaning the highest level of disability.
|
Oswestry Disability Index will be carried out three times (before the start of the therapy, after 4 days of therapy, immediately after its completion and four weeks after the end of the treatment
|
Collaborateurs et enquêteurs
Les enquêteurs
- Chaise d'étude: Kamil Zaworski, Ph.D., John Paul II University of Applied Sciences in Biala Podlaska
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- PopeJohnPaulIIStateSchHigherE2
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .