Access to a Sit-stand Computer Workstation and Back Pain
6. Oktober 2017 aktualisiert von: 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.
Studienübersicht
Status
Abgeschlossen
Bedingungen
Intervention / Behandlung
Studientyp
Interventionell
Einschreibung (Tatsächlich)
57
Phase
- Unzutreffend
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
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California
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Stanford, California, Vereinigte Staaten, 94305
- Stanford University
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
18 Jahre und älter (Erwachsene, Älterer Erwachsener)
Akzeptiert gesunde Freiwillige
Nein
Studienberechtigte Geschlechter
Alle
Beschreibung
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
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
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Kein Eingriff: 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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Experimental: 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.
Andere Namen:
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Change in Back Pain
Zeitfenster: Baseline (Week 1) and Follow-Up (Week 18)
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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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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Change in Pain in Other Body Parts
Zeitfenster: 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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Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Ermittler
- Hauptermittler: Kathleen C Horst, MD, Stanford University
Publikationen und hilfreiche Links
Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.
Allgemeine Veröffentlichungen
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- Hwang JA, Bae SH, Do Kim G, Kim KY. The effects of sensorimotor training on anticipatory postural adjustment of the trunk in chronic low back pain patients. J Phys Ther Sci. 2013 Sep;25(9):1189-92. doi: 10.1589/jpts.25.1189. Epub 2013 Oct 20.
- Zemp R, Taylor WR, Lorenzetti S. In vivo spinal posture during upright and reclined sitting in an office chair. Biomed Res Int. 2013;2013:916045. doi: 10.1155/2013/916045. Epub 2013 Sep 24.
- Lee SH, Kim TH, Lee BH. The effect of abdominal bracing in combination with low extremity movements on changes in thickness of abdominal muscles and lumbar strength for low back pain. J Phys Ther Sci. 2014 Jan;26(1):157-60. doi: 10.1589/jpts.26.157. Epub 2014 Feb 6.
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- Tekur P, Nagarathna R, Chametcha S, Hankey A, Nagendra HR. A comprehensive yoga programs improves pain, anxiety and depression in chronic low back pain patients more than exercise: an RCT. Complement Ther Med. 2012 Jun;20(3):107-18. doi: 10.1016/j.ctim.2011.12.009. Epub 2012 Jan 28.
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- Hartvigsen J, Leboeuf-Yde C, Lings S, Corder EH. Is sitting-while-at-work associated with low back pain? A systematic, critical literature review. Scand J Public Health. 2000 Sep;28(3):230-9.
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- Husemann B, Von Mach CY, Borsotto D, Zepf KI, Scharnbacher J. Comparisons of musculoskeletal complaints and data entry between a sitting and a sit-stand workstation paradigm. Hum Factors. 2009 Jun;51(3):310-20. doi: 10.1177/0018720809338173.
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Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn
1. April 2013
Primärer Abschluss (Tatsächlich)
1. Dezember 2013
Studienabschluss (Tatsächlich)
1. März 2014
Studienanmeldedaten
Zuerst eingereicht
21. Mai 2014
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
21. Mai 2014
Zuerst gepostet (Schätzen)
23. Mai 2014
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
6. November 2017
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
6. Oktober 2017
Zuletzt verifiziert
1. Oktober 2017
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- SSCWStanford
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