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Adjusting Wheelchair Set-Up to Minimize Shoulder Joint Forces During Propulsion

4. november 2008 opdateret af: Kessler Foundation

Computationally Quantifying Wheelchair Set-Up to Minimize Peak Shoulder Joint Forces Throughout Manual Wheelchair Propulsion: A Pilot Study

Individuals who use a manual wheelchair depend upon their upper limbs to provide a means of locomotion during completion of their activities of daily living. As a result of greater than normal usage of the upper limbs, shoulder pain and pathology is common among manual wheelchair users. Accordingly, proper wheelchair set-up may be paramount to preventing injuries and maintaining comfort during locomotion.

The purpose of this research study is to create a subject-specific computer model of wheelchair propulsion to provide information on wheelchair set-up (in particular, axle placement). The primary objective of this study is to investigate the effect of wheelchair set-up on shoulder joint forces during wheelchair propulsion; the secondary objective is to develop a predictive model to identify differences in shoulder joint forces that result from altering the axle position and seating set-up in user's wheelchairs.

The hypothesis of the study is that outputs from a patient-specific model will reveal that the current axle position for each subject results in peak shoulder joint forces that are greater than those predicted from an altered axle position (determined by the model). The overall goal is to then adjust each manual wheelchair user's axle placement to one that minimizes the magnitude of shoulder joint forces throughout propulsion. It is intended that in doing so, the repetitive strain injuries associated with manual wheelchair propulsion may be reduced, prolonging a pain-free way of life for this population.

Studieoversigt

Status

Ukendt

Undersøgelsestype

Observationel

Tilmelding (Forventet)

9

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

    • New Jersey
      • West Orange, New Jersey, Forenede Stater, 07052
        • Rekruttering
        • Kessler Medical Rehabilitation Research and Education Center
        • Underforsker:
          • Trevor A. Dyson-Hudson, M.D.
        • Kontakt:
        • Kontakt:
        • Ledende efterforsker:
          • Sarah R. Dubowsky, Ph.D.
        • Underforsker:
          • Gail F. Forrest, Ph.D.
        • Underforsker:
          • Andrew M. Kwarciak, M.S.
        • Underforsker:
          • Mathew B. Yarossi, B.S.
        • Underforsker:
          • Arvind Ramanujam, M.S.

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 65 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

The racial, gender and ethnic characteristics of the proposed subject population reflects the demographics of Northern New Jersey and the surrounding area and/or the patient population of the Kessler Medical Rehabilitation Research and Education Center (KMRREC). Subjects will be recruited from database search and word of mouth.

Beskrivelse

Experienced Wheelchair Users:

Inclusion Criteria:

  • Have a neurological impairment secondary to a spinal cord injury which occurred over 1 year prior to the start of the study;
  • SCI at or below T1 (complete or incomplete);
  • Use a manual wheelchair as a primary means of mobility (at least 40 hrs. per week but not necessarily always in motion);
  • SCI after age 18
  • Have 24 inch diameter wheels with quick-release axles.

Exclusion Criteria:

  • History of fractures or dislocations in the arms including the shoulder, elbow, and wrist;
  • Upper limb dysthetic pain as a result of a syrinx or reflex sympathetic dystrophy;
  • Pregnant women;
  • Shoulder pain that a MWU describes as limiting their ability to propel a manual wheelchair;
  • History of neurologic disorder other than spinal cord injury (e.g. brain injury).

Inexperienced Manual Wheelchair Users:

Inclusion Criteria:

  • Be between the ages of 18 and 65 years of age.

Exclusion Criteria:

  • History of fractures or dislocations in the arms including the shoulder, elbow, and wrist;
  • Have a musculoskeletal disorder;
  • Pregnant women;
  • Shoulder pain that limits their ability to propel a manual wheelchair.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Kohorter og interventioner

Gruppe / kohorte
1
Able-bodied participants: Able-bodied individuals will be asked to propel a wheelchair at a self-selected speed for a period of time during which data will be collected on their propulsion biomechanics. It is assumed, for the purpose of the study, that un-learned able-bodied individuals learning to propel a wheelchair reflect newly injured individuals who are just getting accustomed to a new chair.
2
Participants with paraplegia: Individuals who are at least 1-year post injury and have used a manual wheelchair as their primary means of locomotion during this time, will be assumed to be, for the purpose of this study, experienced wheelchair users.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Peak shoulder joint forces
Tidsramme: During the propulsive phase of the push stroke at the time of data collection
During the propulsive phase of the push stroke at the time of data collection

Sekundære resultatmål

Resultatmål
Tidsramme
Propulsion Speed
Tidsramme: Measured during the data collection process
Measured during the data collection process
Horizontal and Vertical Axle Placement
Tidsramme: Measured prior to data collection on each test day
Measured prior to data collection on each test day

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Sarah R. Dubowsky, Ph.D., Kessler Medical Rehabilitation Research and Education Center

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. juli 2008

Primær færdiggørelse (Forventet)

1. oktober 2009

Studieafslutning (Forventet)

1. juli 2010

Datoer for studieregistrering

Først indsendt

4. november 2008

Først indsendt, der opfyldte QC-kriterier

4. november 2008

Først opslået (Skøn)

5. november 2008

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

5. november 2008

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

4. november 2008

Sidst verificeret

1. november 2008

Mere information

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Paraplegi

3
Abonner