Access to a Sit-stand Computer Workstation and Back Pain
6 octobre 2017 mis à jour par: Kathleen Horst, Stanford University
Evaluating Change in Back Pain From Access to a Sit-stand Workstation
The purpose of the study is to evaluate the changes in back pain from access to a sit-stand workstation.
Other muscle and joint pain and/or discomfort will also be evaluated.
We hypothesize that access to a sit-stand workstation will allow one to experience postural variation and reduce back pain.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Réel)
57
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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-
California
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Stanford, California, États-Unis, 94305
- Stanford University
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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
18 ans et plus (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Non
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
- Back pain lasting ≥3 months and reported at a minimum of 4 out of 10 on the pain scale.
- Sits >6 hours out of an 8-hour work day for work purposes
- Able and willing to fill out a daily survey for the first week prior to randomization
- Participants must be >18 years of age. There are no gender/race-ethnic restrictions.
- Ability to understand and the willingness to sign a written informed consent document.
Exclusion Criteria:
- Unable to stand for at least 10 minutes.
- Currently using a sit-stand desk
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 parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Aucune intervention: Control
Did not receive an intervention during the active portion of the study (i.e. 12 weeks).
After the active portion of the study, this group was given a sit-stand computer workstation.
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Expérimental: Sit-stand computer workstation
Given a sit-stand computer workstation to use at their place of work
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A sit-stand computer workstation allows one to sit or stand throughout the day while maintaining continued use of one's computer.
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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Change in Back Pain
Délai: Baseline (Week 1) and Follow-Up (Week 18)
|
The Roland-Morris Disability Questionnaire is designed to assess self-rated physical disability caused by low back pain.
The patient is asked to agree or disagree with 24 different statements related to their back pain.
The end score is the sum of the agreed statements.
The score ranges from 0 (no disability) to 24 (maximum disability).
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Baseline (Week 1) and Follow-Up (Week 18)
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in Pain in Other Body Parts
Délai: At the conclusion of each work day for 12 weeks and 8 weeks later
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The Brief Pain Inventory (BPI) allows patients to rate the severity of their pain and the degree to which their pain interferes with common dimensions of feeling and function.
This data was not analyzed due to the focus of the project on lower back pain.
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At the conclusion of each work day for 12 weeks and 8 weeks later
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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: Kathleen C Horst, MD, Stanford University
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
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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
1 avril 2013
Achèvement primaire (Réel)
1 décembre 2013
Achèvement de l'étude (Réel)
1 mars 2014
Dates d'inscription aux études
Première soumission
21 mai 2014
Première soumission répondant aux critères de contrôle qualité
21 mai 2014
Première publication (Estimation)
23 mai 2014
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
6 novembre 2017
Dernière mise à jour soumise répondant aux critères de contrôle qualité
6 octobre 2017
Dernière vérification
1 octobre 2017
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- SSCWStanford
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