- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT00890669
Treadmill Training and Quality of Life in Parkinson's Disease
Treadmill Walking Training With Additional Body Load Improves Quality of Life in Subjects With Parkinson's Disease
Parkinson's disease (PD) causes motor and non-motor impairments that affect the quality of life of the subjects. The purpose was to assess the effects of treadmill walking training with additional body load on the quality of life and motor symptoms of the subjects with PD.
Methods: Nine subjects with PD, Hoehn and Yahr stages 2 through 3, not demented and with capability to ambulate independently voluntarily participate in this study. The training program was divided into three phases (A1-B-A2): treadmill training with additional body load (A1), control condition (conventional physical therapy group) (B) and treadmill training with load again (A2). Each phase lasted six weeks. The quality of life and motor symptoms were assessed by PDQ-39 and UPDRS, respectively. Both evaluations and training were performed during on-phase of the medication cycle.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
SP
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São Carlos, SP, Brasil, 13565-905
- Universidade Federal de Sao Carlos
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Hoehn and Yahr (H-Y) stages 2 through 3
- Absence of dementia (Mini-Mental Status Examination - MMSE, defined according to educational level)
- Capacity to ambulate independently for at least 10 meters
Exclusion Criteria:
- Change medication (dopaminergic) during the study period
- Use treadmill for at least six months prior to the study
- Other neurologic problems or musculoskeletal, cardiovascular and respiratory disease or uncorrected visual deficit that could represent risk and interfere in the accomplishment of the training
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Eksperimentell: PD Group
Nine subjects with idiopathic PD, previously diagnosed by one specialist physician participated in this study.
|
The training program was divided into three phases (A1-B-A2):
Each phase lasted six weeks, totaling 18 weeks. Both evaluations and training were performed during on-phase of the medication cycle. |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
The quality of life was measured through Parkinson Disease Questionnaire (PDQ-39).
Tidsramme: 4 times, once before treatment, and 3 after each treatment phase.
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4 times, once before treatment, and 3 after each treatment phase.
|
Samarbeidspartnere og etterforskere
Etterforskere
- Hovedetterforsker: Nadiesca T Filippin, MSc, Universidade Federal de Sao Carlos
- Studiestol: Rosana Mattioli, PhD, Universidade Federal de Sao Carlos
- Studieleder: Paula H Lobo da Costa, PhD, Universidade Federal de Sao Carlos
Studierekorddatoer
Studer hoveddatoer
Studiestart
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 234/07
- CEP/UFSCar
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