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Non Invasive Ventilation for Acute Exacerbations in Adult CF (NIVinCF)

21. marts 2017 opdateret af: Susan C Johnson, Manchester Metropolitan University

A Mixed Methods Study Comparing the Clinical Efficacy With the Patient Experience of Non-invasive Ventilation During an Acute Exacerbation Complicated by Respiratory Failure in Adult Cystic Fibrosis

Cystic Fibrosis (CF) is a life limiting illness. Median predicted UK survival is 41.4 years (UK CF Registry 2011). The commonest cause of death is respiratory failure.

Non invasive ventilation (NIV) is a system which delivers a preset pressure to supplement the size and depth of each breath. It is introduced in CF to manage established respiratory failure. A nose or a mask which covers both the nose and mouth allows flexible ventilation, is used just at night, or for part of the day in addition or for 24 hours as clinical status indicates. It is introduced within a normal ward environment and then continued longterm at home.Once respiratory failure is established longterm noninvasive ventilation is introduced throughout 24 hours and multidisciplinary assessment concludes that the timing is appropriate for the individual.

This study aims to evaluate a potential development of current practice: the use of non invasive ventilation during hospital admission only to enhance recovery from an acute exacerbation which has caused respiratory failure in those individuals where long term non invasive ventilation is not yet indicated. A mixed methods design will allow description of the experience of noninvasive ventilation during a semistructured interview to add to understanding of the results from an experiment designed to measure the differences between noninvasive ventilation and standard care.

Aim: To compare the clinical efficacy with the patient experience of NIV on recovery from an acute respiratory exacerbation complicated by respiratory failure in adult Cystic Fibrosis.

Studieoversigt

Detaljeret beskrivelse

Design: The study will use a mixed methodology and it will be in 2 phases. Phase I A group randomised controlled trial

The following measurements will be performed on days 1, 3, 7, 10, 14 and twice weekly until discharge:

The exact timing of measurements will be planned by the participant and the researcher.

All of the outcome measures form part of routine clinical practice except the symptom score; the Cystic Fibrosis Respiratory Symptoms Diary (CFRSD V2.0) (Goss et al., 2009)

  1. Early morning and day time carbon dioxide (CO2) level.
  2. Day time oxygen levels
  3. Lung function Forced Expiratory Volume in 1 second (FEV1) and Forced Vital Capacity (FVC)
  4. Day time resting Respiratory Rate (RR), Heart Rate (HR)
  5. Symptom score CFRSD

Phase II A qualitative exploration of the experience of using NIV for adults with Cystic Fibrosis during an acute exacerbation

Methods: Prior to discharge a semistructured interview designed to explore the experience of using noninvasive ventilation will be undertaken by a clinical psychologist from the Cystic Fibrosis multidisciplinary team. The interviews will be undertaken purely for the research project, recorded and transcribed verbatim by the lead investigator. Thematic analysis will be undertaken to interpret and explore the individual's experience. Credibility checking of interpretation will be undertaken by the clinical psychologists and within academic supervision sessions.

Undersøgelsestype

Interventionel

Tilmelding (Forventet)

16

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

    • Manchester
      • Wythenshawe, Manchester, Det Forenede Kongerige, M23 9LT
        • Rekruttering
        • Manchester Adult Cystic Fibrosis Centre, University Hospitals South Manchester
        • Ledende efterforsker:
          • Susan C Johnson, MSc MCSP

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 og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Adult Cystic Fibrosis
  • Hospital admission to Pearce Ward Manchester Adult Cystic Fibrosis Centre
  • Acute respiratory exacerbation conforming with a standard definition of pulmonary exacerbation (Fuchs et al 1994).
  • An admission day time CO2 > 6 kilopascal (kPa) on standard therapy
  • Freely given informed consent.-
  • 24.3.15 substantial amendment approval for an admission early morning CO2 > 6 kPa

Exclusion Criteria:

  • A day time CO2 >8.0 kPa
  • respiratory acidosis
  • clinical exclusion by CF consultant physician or clinical psychologist

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Støttende pleje
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Non invasive ventilation (NIV)
Non invasive ventilation used for the first 7 days of study
Andre navne:
  • NIV
  • Non-invasiv ventilation
Aktiv komparator: Standard Care
High Flow Controlled Oxygen Therapy

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Change in day time carbon dioxide (CO2)
Tidsramme: Day 7
Day 7

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Early morning oxygen (O2) and CO2 levels
Tidsramme: days 1,3,5,7,10 and 14
days 1,3,5,7,10 and 14
Lung function (FEV1 and FVC)
Tidsramme: Day 7, 14
Day 7, 14
Respiratory Rate
Tidsramme: days 1,3,5,7,10 and 14
days 1,3,5,7,10 and 14
Heart Rate
Tidsramme: Days 1,3,5,7,10 and 14
Days 1,3,5,7,10 and 14
Symptom score (CFRSD)
Tidsramme: days 1,3,5,7,10 and 14
Cystic Fibrosis Respiratory Symptom Diary (Daily Recall)
days 1,3,5,7,10 and 14

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Semi structured interview
Tidsramme: Day 14
Psychologist delivered semi structured interview discussing participant experience of non invasive ventilation (NIV)
Day 14

Samarbejdspartnere og efterforskere

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

Efterforskere

  • Ledende efterforsker: Susan C Johnson, MSC MCSP, Manchester Adult Cystic Fibrosis Centre, University Hospitals South Manchester

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. august 2014

Primær færdiggørelse (Forventet)

1. september 2017

Studieafslutning (Forventet)

1. september 2017

Datoer for studieregistrering

Først indsendt

5. september 2014

Først indsendt, der opfyldte QC-kriterier

8. september 2014

Først opslået (Skøn)

9. september 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

22. marts 2017

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

21. marts 2017

Sidst verificeret

1. marts 2017

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 .

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