SEGMENTAL AND GENERAL STABILIZATION EXERCISES IN CHRONIC LOW BACK PAIN
9 octobre 2021 mis à jour par: Isra University
SEGMENTAL STABILIZATION AND GENERAL LUMBER STABILIZATION EXERCISE IN CHRONIC LOW BACK PAIN
Chronic low back pain effects more than 50% of general population. It's prevalence is higher is young adults that are economically active adults.
Its significance is often underestimated because usually young adults ignore these initial episodes of low back pain due to their busy life style or life full of commitments. Approximately 70% of adults have at least one episode of low back pain during their lifetimes.
Aperçu de l'étude
Statut
Complété
Intervention / Traitement
Description détaillée
It will be randomized control trial with 60 patients with chronic low back pain divided into 2 groups.
One group will be given segmental stabilization whose purpose is to achieve segmental control over primary stabilizers.
Second group will be given just generalized lumber stabilization exercises as it includes close chain exercises with low velocity as well as low load.
This study will be conducted in Rehabilitation setup of Benazir Bhutto hospital Rawalpindi and IIRS that is Rehabilitation dept.
at Al Nafees medical college and hospital, Islamabad.
Non probability Convenience Sampling technique will be utilized
Type d'étude
Interventionnel
Inscription (Réel)
44
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
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Islamabad, Pakistan, 44950
- Isra Institute of Rehabilitation Sciences
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
15 ans à 60 ans (Enfant, Adulte)
Accepte les volontaires sains
Oui
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
- Both males and females will be included in the study
Exclusion Criteria:
- Age limits of subjects will be between 15 to 60
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation séquentielle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
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Expérimental: Segmental Stabilization
Segmental control over the primary stabilizers (TrA, deep multifidus, pelvic floor and diaphram) is maintained.
Weight of body is minimized by using drawing in maneuver.
Time duration will be of 30 to 40 mins, thrice a week for four weeks.
Hot packs will be applied for 10 mins.
In starting days, 8 to 10 reps with hold time 5 count.
In later days, 12 to 15 reps with hold time increases up till 10 to 15 counts.
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Physiotherapist will perform activation of multifidus in prone position.
It also includes activation of transverse abdominas in crook lying position, in sitting as well as in point kneeling position to re-establish simultaneous contraction of deep muscles synergy.
Autres noms:
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Comparateur actif: General lumber stabilization exercises
It includes exercises in closed chain with low velocity as well as low load.
Time duration will be of 30 to 40 mins, thrice a week for four weeks.
Hot packs will be applied for about 10 mins.
In starting days, 8 to 10 reps with hold time 5 count.
In later days, 12 to 15 reps with hold time increases up till 10 to 15 counts.
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It can by performed by patient him or her self under physiotherapist's assistance.
Lumber neutral position is maintained.
Bridging in prone as well as supine position will be maintained.
Autres noms:
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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VAS
Délai: 4 weeks (1st reading is at the baseline, 2nd is at 3rd day, 3rd is at 5th day, 4th is at 8th day, 5th is at 10th day, 6th is at 12th day, 7th is at 19th day and 8th reading is at 26th day.
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Visual analogue scale for Pain 0= no pain, 10= unbearable pain
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4 weeks (1st reading is at the baseline, 2nd is at 3rd day, 3rd is at 5th day, 4th is at 8th day, 5th is at 10th day, 6th is at 12th day, 7th is at 19th day and 8th reading is at 26th day.
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Oswestry disability Index
Délai: 4 weeks (1st reading is at the baseline, 2nd is at 3rd day, 3rd is at 5th day, 4th is at 8th day, 5th is at 10th day, 6th is at 12th day, 7th is at 19th day and 8th reading is at 26th day.
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It is used to measure permanent functional disability.
For each section, total possible score is 5, after completing all 10 sections.
sum of all scores will be obtained in the form of percentages.
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4 weeks (1st reading is at the baseline, 2nd is at 3rd day, 3rd is at 5th day, 4th is at 8th day, 5th is at 10th day, 6th is at 12th day, 7th is at 19th day and 8th reading is at 26th day.
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International physical activity questionnaire
Délai: Only one reading is required that is the baseline reading.
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It is used to measure to physical activity of a person
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Only one reading is required that is the baseline reading.
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Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
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ROM
Délai: 4 weeks (1st reading is at the baseline, 2nd is at 3rd day, 3rd is at 5th day, 4th is at 8th day, 5th is at 10th day, 6th is at 12th day, 7th is at 19th day and 8th reading is at 26th day.
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It is an acronym of Range of motion
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4 weeks (1st reading is at the baseline, 2nd is at 3rd day, 3rd is at 5th day, 4th is at 8th day, 5th is at 10th day, 6th is at 12th day, 7th is at 19th day and 8th reading is at 26th day.
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Dr. Summaiya Zaman, Mphil, Isra Institute of rehabilitation
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
26 mars 2019
Achèvement primaire (Réel)
11 novembre 2020
Achèvement de l'étude (Réel)
11 décembre 2020
Dates d'inscription aux études
Première soumission
9 avril 2020
Première soumission répondant aux critères de contrôle qualité
9 octobre 2021
Première publication (Réel)
12 octobre 2021
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
12 octobre 2021
Dernière mise à jour soumise répondant aux critères de contrôle qualité
9 octobre 2021
Dernière vérification
1 avril 2020
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 1703-MPHIL-OPT/008
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
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 .