- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01690273
Exercise Therapy Program in Ankylosing Spondylitis Patients
27. august 2016 oppdatert av: Andrea Lopes Gallinaro, University of Sao Paulo
Effect of Two Exercise Therapy Program With and Without Elastic Resistance in Ankylosing Spondylitis Patients
Mobility exercises are used in Ankylosing Spondylitis (AS) patients to preserve and restore axial mobility, but there are no data regarding a specific rehabilitation program that includes flexibility alone and its association with resistance exercises in AS patients with stable disease activity.
So, we assessed the effects of two exercise programs in terms of mobility, functional capacity, quality of life and disease activity in AS patients.
Methods.
Fifty-five sedentary AS patients with a Bath Ankylosing Spondylitis Activity Index (BASDAI) <4 were included.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
The AS patients were randomly assigned into three groups, to receive a mobility exercise program (M) or mobility plus elastic resistance exercise program (M+R) or no exercise (C).
The exercises group sessions were conducted twice per week for 16 weeks.
This supervised program comprised 30 minutes of outdoor stretching and mobility exercises for the spine and limbs (M).
After the flexibility program, M+R group carry out more 30 minutes of elastic resistance exercises.
The mobility, disease activity and functional parameters were evaluated at baseline and after 16 weeks, with the evaluator blinded to the treatment group.
Studietype
Intervensjonell
Registrering (Faktiske)
55
Fase
- Ikke aktuelt
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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Sao Paulo, Brasil, 05403-010
- University of Sao Paulo
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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
- Barn
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Ankylosing spondylitis patient
- Basdai index lower than 4
- Physical inactive
- Functional class I to III
Exclusion Criteria:
- Fibromyalgia
- Cardiovascular disease
- Pain Visual Analogue Scale ("VAS") over 8
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Støttende omsorg
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Ingen inngripen: ankylosing spondylitis control
control group
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Eksperimentell: mobility exercise
mobility exercises
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30 minutes, twice a week
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Eksperimentell: mobility and elastic resistance exercise
AS patients was submitted to a program mobility exercise plus elastic resistance exercises
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30 minutes, twice a week each exercises group.
(total 1 hour)
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
FUNCTIONAL INDEX
Tidsramme: Baseline and 16 Weeks
|
BASFI - Bath ankylosing spondylitis functional index.
A scale from 0 to 10 (lower scores means better functional capacity), results are measured by mean and standard deviation.
|
Baseline and 16 Weeks
|
Mobility Index
Tidsramme: Baseline and 16 weeks
|
Bath ankylosing spondylitis motion index.
A mean of five mobility measures committed by Ankylosing Spondylitis disease.
Higher results means higher limitations in mobility (units of measure from 0 to 10)
|
Baseline and 16 weeks
|
Disease Activity Index
Tidsramme: Baseline and 16 Weeks
|
BASDAI - Bath ankylosing spondylitis disease activity index.
Scale from 0 to 6. Higher scores means worst disease activity.
Numbers are expressed in average (SD)
|
Baseline and 16 Weeks
|
Ankylosing Spondylitis Disease Activity Scale -Disease Activity
Tidsramme: Baseline and 16 Weeks
|
Scores vary from 0 to 10, and higher than 4 scores are indicative of disease activity.
Data are expressed by means and SD
|
Baseline and 16 Weeks
|
Global Evaluation Self Reported
Tidsramme: Baseline and 16 Weeks
|
Bath Ankylosing Spondylitis Global is a self reported global score varying from 0 to 10. Higher scores means worst health evaluation.
Expressed by means and standard deviation.
|
Baseline and 16 Weeks
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Thoracolumbar Mobility
Tidsramme: Baseline and 16 Weeks
|
Thoracolumbar rotation Pavelka.
Measured with a tape in centimeters.
Higher number means better thoracolumbar rotation
|
Baseline and 16 Weeks
|
Pain Scale
Tidsramme: Baseline and 16 Weeks
|
Pain was evaluated in a visual analogue scale (VAS) from 0 to 10. higher scores means much pain.
Data was expressed by means and standard deviation.
|
Baseline and 16 Weeks
|
Stiffness Scale
Tidsramme: Baseline and 16 Weeks
|
Stiffness was measured by an VAS varying from 0 to 10. Higher scores means worst stiffness.
Data are expressed by mean and SD.
|
Baseline and 16 Weeks
|
Short Form-12 (PCS)
Tidsramme: Baseline and 16 Weeks
|
Quality of life was analyzed in a physical component score varying from 0 (lowest level of health) to 100 (highest level of health) scale.
Data are expressed by mean and SD.
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Baseline and 16 Weeks
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Short Form-12 (MCS)
Tidsramme: Baseline and 16 Weeks
|
Quality of life was analyzed in a mental component score varying from 0 (lowest level of health) to 100 (highest level of health).
Data are expressed by mean and SD.
|
Baseline and 16 Weeks
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MASES
Tidsramme: Baseline and 16 Weeks
|
Maastricht Ankylosing Spondylitis Enthesitis Score (MASES) score varying from 0 to 13.
Where 0 is no painful point reported and 13 is all tender points reported as painful.
Data are expressed by means and standard deviation
|
Baseline and 16 Weeks
|
Chin-coronoid Distance
Tidsramme: Baseline and 16 Weeks
|
lateral rotation of the head (chin-coronoid distance) was measured with a tape in centimeters.
Highest score means better lateral rotation mobility.
Data are expressed by means and standard deviation
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Baseline and 16 Weeks
|
Tragus-coronoid Distance
Tidsramme: Baseline and 16 Weeks
|
lateral flexion of the head (tragus-coronoid distance) was measured with a tape in centimeters.
Highest score means better lateral flexion mobility of the head.Data are expressed by means and standard deviation
|
Baseline and 16 Weeks
|
Finger Floor Distance
Tidsramme: Baseline and 16 Weeks
|
Distance between third finger of the hand and the floor while in lumbar flexion.
It was measured with a tape in centimeters.
Highest score means better torso flexion mobility.
Data are expressed by means and standard deviation
|
Baseline and 16 Weeks
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Chest Expansion
Tidsramme: Baseline and 16 Weeks
|
Chest expansion was measured with a tape in centimeters between inspiration and breathing exhaling.
Highest score means better chest expansion.
Data are expressed by means and standard deviation.
|
Baseline and 16 Weeks
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Studiestol: Ana Lucia Pinto, Phd, University of Sao Paulo
Publikasjoner og nyttige lenker
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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. juli 2012
Primær fullføring (Faktiske)
1. juni 2013
Studiet fullført (Faktiske)
1. november 2014
Datoer for studieregistrering
Først innsendt
18. september 2012
Først innsendt som oppfylte QC-kriteriene
20. september 2012
Først lagt ut (Anslag)
21. september 2012
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
20. oktober 2016
Siste oppdatering sendt inn som oppfylte QC-kriteriene
27. august 2016
Sist bekreftet
1. august 2016
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 8206212
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
JA
IPD-planbeskrivelse
paper is been written
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