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Study of Body Positions in Unconsciousness

8 oktober 2020 uppdaterad av: University of Oxford

A Randomised Controlled Study of the Use of Recovery Positions for Comatose Patients in a Resource Limited Setting

In resource limited settings, access to one-on-one nursing care and airway protection by intubation may be unavailable. Patients with coma but adequate oxygenation are frequently cared for on medical wards, and nursed by their family members. The investigators previously audited the use of the recovery position in patients with cerebral malaria and found that its usage was greatly increased by an educational intervention aimed at patient's caregivers. A trend to reduction in coma duration and aspiration pneumonia was also found. Since there is no evidence that placing comatose, non-intubated patients in a recovery position improves outcome, the investigators plan to conduct a randomised controlled study comparing standard care with an educational intervention targeting patients' relatives, teaching them to maintain their relative in one of two different recovery positions. With the preliminary efficacy and safety data and feedback that this study will provide, the investigators would then move to conduct a large multicenter study powered to detect a difference in mortality.

Studieöversikt

Detaljerad beskrivning

Methods:

In this prospective, three-armed randomised controlled study, patients admitted to the adult medical wards of Chittagong Medical College Hospital with acute onset of reduced consciousness (Glasgow Coma Scale (GCS) <12 for less than 5 days) will be randomised 1:1:1 to one of three arms; standard care (no intervention) or an educational intervention directing placement into one of two recovery positions.

The educational intervention will occur following randomisation and on daily follow-up until recovery from deep coma or death. For patients in the intervention arms, the patients' relatives will be instructed on how to maintain their patient in the recovery position, and an educational poster will be attached to their bed.

Enrolled subjects will be observed 3 times a day until discharge for body position and vital signs including GCS, heart rate, respiratory rate and oxygen saturation.

The primary outcome will be the risk of (hazard ratio) aspiration pneumonia and pneumonitis. The secondary outcome measures will include time to hypoxia, death and coma recovery time. Pulmonary complications will be defined clinically and radiologically. The primary comparison between groups will be the standard care group versus both recovery positions combined. Analysis will be by intention to treat.

Studietyp

Interventionell

Inskrivning (Faktisk)

1540

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Chittagong, Bangladesh
        • Chittagong medical College hospital

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • Male or female admitted to the medical wards at CMCH
  • Current GCS < 12
  • Less than 5 day history of reduced consciousness
  • Written informed consent obtained through an adult (≥18 years) relative or parent/guardian

Exclusion Criteria:

  • Suspected head or spinal injury/trauma requiring appropriate immobilisation and stabilization
  • Patient physically restrained by ward staff due to agitation
  • Unsuitability for lateral positioning e.g. due to burns on lateral aspects, femoral vascular catheter
  • Requirement for nursing in an upright position e.g. due to respiratory insufficiency
  • Known or suspected pregnancy
  • Intubation
  • Patient or family member previously enrolled in this study.
  • Consent refused, or no adult (≥18 years) relative or parent/guardian present to give consent

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Stödjande vård
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Inget ingripande: Control
Randomized to standard care (control group) - observations only
Experimentell: UKRC 1997
Randomized to modified UKRC 1997 - Intervention and Observations
Educational poster intervention indicating the modified UKRC 1997 recovery position
Experimentell: UKRC 2010
Randomized to modified UKRC 2010 - Intervention and Observations
Educational poster intervention indicating the modified UKRC 2010 recovery position

Vad mäter studien?

Primära resultatmått

Resultatmått
Tidsram
Composite of aspiration pneumonitis or pneumonia
Tidsram: 48 hours after GCS13
48 hours after GCS13

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Proportion of patients developing hypoxia
Tidsram: 48 hours after GCS13,
48 hours after GCS13,
Development of pneumonia or pneumonitis, assessed individually
Tidsram: 48 hours after GCS13
48 hours after GCS13
Mortality
Tidsram: 7 days post discharge/last follow-up
7 days post discharge/last follow-up
Time to mortality
Tidsram: 7 days post discharge/last follow-up
7 days post discharge/last follow-up
Coma recovery time, defined as time to GCS 15
Tidsram: during hospitalization (defined as time to GCS 15), expected less than 4 weeks
during hospitalization (defined as time to GCS 15), expected less than 4 weeks
The number of documented episodes of hypoxia
Tidsram: 48 hours after GCS 13
48 hours after GCS 13
Percentage of observations in the recovery position
Tidsram: whilst GCS<12, expected less than 2 months
whilst GCS<12, expected less than 2 months
Modified Rankin scale
Tidsram: on discharge, expected less than 2 months
on discharge, expected less than 2 months
Composite of pressure sore, venous thrombosis, arm or leg peripheral nerve or joint injury
Tidsram: whilst GCS<12, expected less than 2 months
whilst GCS<12, expected less than 2 months
Proportion of patients developing a pressure sore
Tidsram: whilst GCS<12, expected less than 2 months
whilst GCS<12, expected less than 2 months
Proportion of patients developing a venous thrombosis,
Tidsram: whilst GCS<12, expected less than 2 months
whilst GCS<12, expected less than 2 months
Proportion of patients developing a new arm or leg peripheral nerve injury
Tidsram: during hospitalization, expected less than 2 months
during hospitalization, expected less than 2 months
Proportion of patients developing a new arm or leg joint injury
Tidsram: during hospitalization, expected less than 2 months
during hospitalization, expected less than 2 months
Trends in Blood presure
Tidsram: during hospitalization, expected less than 2 months
measure Systolic and diastolic blood pressure levels
during hospitalization, expected less than 2 months
Trends in heart rate
Tidsram: during hospitalization, expected less than 2 months
during hospitalization, expected less than 2 months
Proportion of patients developing peripheral venous cannula function
Tidsram: whilst GCS<12, expected less than 2 months
whilst GCS<12, expected less than 2 months
time to hypoxia
Tidsram: 48 hours after GCS13, expected less than 2 months
48 hours after GCS13, expected less than 2 months

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Hugh Kingston, Dr., Mahidol Oxford Tropical Medicine Research Unit

Publikationer och användbara länkar

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Allmänna publikationer

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

23 augusti 2014

Primärt slutförande (Faktisk)

21 mars 2020

Avslutad studie (Faktisk)

21 mars 2020

Studieregistreringsdatum

Först inskickad

12 januari 2015

Först inskickad som uppfyllde QC-kriterierna

27 april 2015

Första postat (Uppskatta)

28 april 2015

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

12 oktober 2020

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

8 oktober 2020

Senast verifierad

1 oktober 2020

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • BAKMAL1405

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