To Evaluate the Effect of Inhaled Medication Together With Exercise and Activity Training on Exercise Capacity and Daily Activities in Patients With Chronic Lung Disease With Obstruction of Airways
9. november 2016 oppdatert av: Boehringer Ingelheim
An Exploratory, 12 Week, Randomised, Partially Double-blinded, Placebo-controlled Parallel Group Trial to Explore the Effects of Once Daily Treatments of Orally Inhaled Tiotropium + Olodaterol Fixed Dose Combination or Tiotropium (Both Delivered by Respimat® Inhaler), Supervised Exercise Training and Behavior Modification on Exercise Capacity and Physical Activity in Patients With Chronic Obstructive Pulmonary Disease (COPD)
The primary objectives of the study are to explore the effect of treatment with orally inhaled tiotropium + olodaterol fixed dose combination with and without exercise training, and tiotropium comparing to placebo, on top of behavioural modification in improving exercise capacity in patients with COPD
Studieoversikt
Status
Fullført
Forhold
Studietype
Intervensjonell
Registrering (Faktiske)
304
Fase
- Fase 3
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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South Australia
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Daw Park, South Australia, Australia
- Boehringer Ingelheim Investigational Site
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Glen Osmond, South Australia, Australia
- Boehringer Ingelheim Investigational Site
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Genk, Belgia
- Boehringer Ingelheim Investigational Site
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Hasselt, Belgia
- Boehringer Ingelheim Investigational Site
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Leuven, Belgia
- Boehringer Ingelheim Investigational Site
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Quebec
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Montreal, Quebec, Canada
- Boehringer Ingelheim Investigational Site
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Ste-Foy, Quebec, Canada
- Boehringer Ingelheim Investigational Site
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Saskatchewan
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Saskatoon, Saskatchewan, Canada
- Boehringer Ingelheim Investigational Site
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Kolding, Danmark
- Boehringer Ingelheim Investigational Site
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København NV, Danmark
- Boehringer Ingelheim Investigational Site
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Odense, Danmark
- Boehringer Ingelheim Investigational Site
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California
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San Diego, California, Forente stater
- Boehringer Ingelheim Investigational Site
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Torrance, California, Forente stater
- Boehringer Ingelheim Investigational Site
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Connecticut
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Hartford, Connecticut, Forente stater
- Boehringer Ingelheim Investigational Site
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Greenlane East Auckland NZ, New Zealand
- Boehringer Ingelheim Investigational Site
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Gdansk, Polen
- Boehringer Ingelheim Investigational Site
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Lodz, Polen
- Boehringer Ingelheim Investigational Site
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Starachowice, Polen
- Boehringer Ingelheim Investigational Site
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Coimbra, Portugal
- Boehringer Ingelheim Investigational Site
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Lisboa, Portugal
- Boehringer Ingelheim Investigational Site
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Porto, Portugal
- Boehringer Ingelheim Investigational Site
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Leicester, Storbritannia
- Boehringer Ingelheim Investigational Site
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Norwich, Storbritannia
- Boehringer Ingelheim Investigational Site
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Sheffield, Storbritannia
- Boehringer Ingelheim Investigational Site
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Berlin, Tyskland
- Boehringer Ingelheim Investigational Site
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Bochum, Tyskland
- Boehringer Ingelheim Investigational Site
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Frankfurt, Tyskland
- Boehringer Ingelheim Investigational Site
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Großhansdorf, Tyskland
- Boehringer Ingelheim Investigational Site
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Heidelberg, Tyskland
- Boehringer Ingelheim Investigational Site
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Leverkusen, Tyskland
- Boehringer Ingelheim Investigational Site
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Solingen, Tyskland
- Boehringer Ingelheim Investigational Site
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Teuchern, Tyskland
- Boehringer Ingelheim Investigational Site
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Tübingen, Tyskland
- Boehringer Ingelheim Investigational Site
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Salzburg, Østerrike
- Boehringer Ingelheim Investigational Site
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
40 år til 75 år (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion criteria:
- All patients must sign an informed consent consistent with International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) - Good Clinical Practice (GCP) guidelines prior to participation in the trial, which includes medication washout and restrictions.
- All patients must have a diagnosis of chronic obstructive pulmonary disease and must meet the following spirometric criteria: Patients must have relatively stable airway obstruction with a post-bronchodilator forced expiratory volume in one second >=30% and <80% of predicted normal; Global Initiative for Chronic Obstructive Lung Disease grade II - III, and a post-bronchodilator Tiffeneau index <70% at Visit 1.
- Male or female patients, aged >=40 years and <=75 years.
- Patients must be current or ex-smokers with a smoking history of more than 10 pack years. Patients who have never smoked cigarettes must be excluded.
Exclusion criteria:
- Patients with a significant disease other than chronic obstructive pulmonary disease.
- Patients with clinically relevant abnormal baseline haematology, blood chemistry, or urinalysis.
- Patients with a history of asthma.
- A diagnosis of thyrotoxicosis.
- A diagnosis of paroxysmal tachycardia (>100 beats per minute).
- A history of myocardial infarction within 1 year of screening visit.
- Unstable or life-threatening cardiac arrhythmia.
- Hospitalized for heart failure within the past year.
- Known active tuberculosis.
- A malignancy for which patient has undergone resection, radiation therapy or chemotherapy within last five years.
- A history of life-threatening pulmonary obstruction and patients with chronic respiratory failure.
- A history of cystic fibrosis.
- Clinically evident bronchiectasis.
- A history of significant alcohol or drug abuse.
- Any contraindications for exercise testing.
- Patients who have undergone thoracotomy with pulmonary resection.
- Patients being treated with any oral ß-adrenergics.
- Patients being treated with oral corticosteroid medication at unstable doses (i.e., less than six weeks on a stable dose) or at doses in excess of the equivalent of 10 mg of prednisone per day or 20 mg every other day.
- Patients who regularly use daytime oxygen therapy for more than one hour per day and in the investigators opinion will be unable to abstain from the use of oxygen therapy during clinic visits.
- Patients who have completed a pulmonary rehabilitation program in the six weeks prior to the screening visit or patients who are currently in a pulmonary rehabilitation program.
- Patients who have a limitation of exercise performance as a result of factors other than fatigue or exertional dyspnoea, such as arthritis in the leg, angina pectoris or claudication or morbid obesity.
- Patients who have taken an investigational drug within one month or six half lives (whichever is greater) prior to screening visit.
- Patients with known hypersensitivity to ß-adrenergics drugs, anticholinergic drugs, benzalkonium chloride, disodium edentat, or any other component of the Respimat® inhalation solution delivery system.
- Pregnant or nursing women.
- Women of childbearing potential not using highly effective methods of birth control.
- Patients who have previously been randomized in this study or are currently participating in another study.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Placebo komparator: placebo
patient will receive placebo once daily, 2 puffs in the morning
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comparator
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Eksperimentell: tiotropium + olodaterol high dose with BM
patient will receive tiotropium 5 mcg + olodaterol 5 mcg in fixed dose combination once daily, 2 puffs in the morning
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olodaterol 5 mcg once daily fixed dose combination
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Aktiv komparator: tiotropium
patient will receive tiotropium 5 mcg once daily, 2 puffs in the morning
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tiotropium 5 mcg once daily fixed dose combination
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Eksperimentell: tiotropium + olodaterol with exercise training and BM
patient will receive tiotropium 5 mcg + olodaterol 5 mcg in fixed dose combination once daily, 2 puffs in the morning
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tiotropium 5 mcg once daily
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
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Endurance Time During Endurance Shuttle Walk Test (ESWT) to Symptom Limitation After 8 Weeks
Tidsramme: Week 8
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Endurance time during ESWT to symptom limitation at walking speed corresponding to 85% of predicted maximum oxygen consumption (VO2 peak) after 8 weeks of pharmacological treatment and non-pharmacological intervention.
The numerical value of endurance time in seconds was transformed in log10 scale to correct for skewness and then an analysis of covariance (ANCOVA) was fitted to the log10-transformed data and the least square means (LSMean) and standard error (SE) were obtained.
To present the results in a way easier for interpretation, the least square mean from the ANCOVA fitted to the log10-transformed data were transformed back taking 10 to the power of the least square estimate to obtain the geometric mean and the corresponding SE was transformed using delta method to get the corresponding SE of the geometric mean.
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Week 8
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
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Average Daily Walking Time Measured by the Activity Monitor in the Week Prior to Week 12
Tidsramme: Week 12
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Average daily walking time measured by the activity monitor in the week prior to Week 12.
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Week 12
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Average Daily Walking Intensity Measured by the Activity Monitor in the Week Prior to 12 Weeks of Treatment
Tidsramme: Week 12
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Average daily walking intensity measured by the activity monitor in the week prior to 12 weeks of treatment.
The Movement Intensity (MI) is derived from the acceleration signals.
Since seismic sensors measure gravitational acceleration (g) in static situations, the acceleration signal is expressed relative to g (1g = 9.81m/s2).
To calculate movement intensity (MI) the gravitational acceleration in static situations was removed and the rotation vector of the three accelerometer signals was calculated.
The MI gives an indication of the power of movements.
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Week 12
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Perceived Difficulties as Evaluated With Functional Performance Inventory-Short Form (FPI-SF) Total Score at Week 12
Tidsramme: Week 12
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Perceived difficulties as evaluated with FPI-SF.
FPI-SF self-report questionnaire has 6 domains: Body care(5 items), Household maintenance(8 items), Physical exercise(5 items), Recreation(5 items), Spiritual activities(4 items) and Social interaction(5 items) with five possible answers on each item: Do with no difficulty - 3, Do with some difficulty - 2, Do with great difficulty - 1, don't do because of health reasons - 0, and don't do because choose not to - 0. Domain scores are expressed as mean values, with at least 6 non-missing items required for the household maintenance domain and at least 3 non-missing items for the other domains.
Total score is the mean across the six domains.
So total and domain scores range from 0 to 3, with higher scores indicating higher levels of functional activity within and across domains.
Respondents engaged in many activities with no difficulty will score high on the FPI, while those who perform few activities with much difficulty will score low.
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Week 12
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Endurance Time During Endurance Shuttle Walk Test (ESWT) to Symptom Limitation After 12 Weeks
Tidsramme: Week 12
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Endurance time during ESWT to symptom limitation at walking speed corresponding to 85% of maximum oxygen consumption (VO2 peak) after 12 weeks of pharmacological treatment and non-pharmacological intervention.
The numerical value of endurance time in seconds was transformed in log10 scale to correct for skewness and then the ANCOVA was fitted to the log10-transformed data and the least square means and SE were obtained.
To present the results in a way easier for interpretation, the least square mean from the ANCOVA fitted to the log10-transformed data were transformed back taking 10 to the power of the least square estimate to obtain the geometric mean and the corresponding SE was transformed using delta method to get the corresponding SE of the geometric mean.
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Week 12
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One Hour, Post-dose Forced Expiratory Volume in One Second (FEV1) After 8 Weeks of Treatment
Tidsramme: Week 8
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One hour, Post-dose Forced Expiratory Volume in One Second (FEV1) after 8 weeks of treatment.
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Week 8
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One Hour, Post-dose Forced Vital Capacity (FVC) After 8 Weeks of Treatment
Tidsramme: Week 8
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One hour, Post-dose Forced Vital Capacity (FVC) after 8 weeks of treatment.
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Week 8
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Resting Inspiratory Capacity (IC) Measured at 1.5 Hours Post Dose After 8 Weeks of Treatment
Tidsramme: Week 8
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Resting inspiratory capacity (IC) measured at 1.5 hours post dose after 8 weeks of treatment.
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Week 8
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Generelle publikasjoner
- Troosters T, Bourbeau J, Maltais F, Leidy N, Erzen D, De Sousa D, Korducki L, Hamilton A. Enhancing exercise tolerance and physical activity in COPD with combined pharmacological and non-pharmacological interventions: PHYSACTO randomised, placebo-controlled study design. BMJ Open. 2016 Apr 13;6(4):e010106. doi: 10.1136/bmjopen-2015-010106.
- Bourbeau J, Lavoie KL, Sedeno M, De Sousa D, Erzen D, Hamilton A, Maltais F, Troosters T, Leidy N. Behaviour-change intervention in a multicentre, randomised, placebo-controlled COPD study: methodological considerations and implementation. BMJ Open. 2016 Apr 4;6(4):e010109. doi: 10.1136/bmjopen-2015-010109.
Hjelpsomme linker
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. mars 2014
Primær fullføring (Faktiske)
1. august 2015
Studiet fullført (Faktiske)
1. oktober 2015
Datoer for studieregistrering
Først innsendt
7. mars 2014
Først innsendt som oppfylte QC-kriteriene
7. mars 2014
Først lagt ut (Anslag)
12. mars 2014
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
6. januar 2017
Siste oppdatering sendt inn som oppfylte QC-kriteriene
9. november 2016
Sist bekreftet
1. november 2016
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Sykdommer i luftveiene
- Lungesykdommer, obstruktiv
- Lungesykdommer
- Lungesykdom, kronisk obstruktiv
- Fysiologiske effekter av legemidler
- Nevrotransmittere agenter
- Molekylære mekanismer for farmakologisk virkning
- Parasympatholytika
- Autonome agenter
- Agenter fra det perifere nervesystemet
- Kolinerge antagonister
- Kolinerge midler
- Bronkodilatatorer
- Anti-astmatiske midler
- Luftveismidler
- Tiotropiumbromid
- Olodaterol
Andre studie-ID-numre
- 1237.16
- 2013-002671-18 (EudraCT-nummer: EudraCT)
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .