SEGMENTAL AND GENERAL STABILIZATION EXERCISES IN CHRONIC LOW BACK PAIN
9 ottobre 2021 aggiornato da: 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.
Panoramica dello studio
Stato
Completato
Intervento / Trattamento
Descrizione dettagliata
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
Tipo di studio
Interventistico
Iscrizione (Effettivo)
44
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
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Islamabad, Pakistan, 44950
- Isra Institute of Rehabilitation Sciences
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
Da 15 anni a 60 anni (Bambino, Adulto)
Accetta volontari sani
Sì
Sessi ammissibili allo studio
Tutto
Descrizione
Inclusion Criteria:
- Both males and females will be included in the study
Exclusion Criteria:
- Age limits of subjects will be between 15 to 60
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione sequenziale
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
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Sperimentale: 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.
Altri nomi:
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Comparatore attivo: 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.
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
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VAS
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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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Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
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ROM
Lasso di tempo: 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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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Investigatori
- Investigatore principale: Dr. Summaiya Zaman, Mphil, Isra Institute of rehabilitation
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Effettivo)
26 marzo 2019
Completamento primario (Effettivo)
11 novembre 2020
Completamento dello studio (Effettivo)
11 dicembre 2020
Date di iscrizione allo studio
Primo inviato
9 aprile 2020
Primo inviato che soddisfa i criteri di controllo qualità
9 ottobre 2021
Primo Inserito (Effettivo)
12 ottobre 2021
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
12 ottobre 2021
Ultimo aggiornamento inviato che soddisfa i criteri QC
9 ottobre 2021
Ultimo verificato
1 aprile 2020
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 1703-MPHIL-OPT/008
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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