- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00611364
Physical Therapy for Hypertensive Elderly
Physical Therapy for Hipertensive Elderly: Effects in the Physical Activity and Exercise Adherence
Physical therapy for hipertensive elderly: effects in the physical activity and exercise adherence.
Introduction: The arterial hypertension (AH) is a clinical syndrome characterized by blood pressure ≥ 140/90mmHg. Practical of physical activity (PA) and/or physical exercise (PE) is one of the modalities of not farmacological treatment. Hypertensive aged not adhere to this recommendation for presenting factors that make it difficult this practical. Objective: to verify if physical therapy (PT) treatment can improve the AF and EF adhesion of hypertensive aged. Methods: The sample was composed by 43 hypertensive aged of Arterial Hypertensive League of the Federal University of Goiás. Of these, 30 had remained in the study and had been randomized in study group (SG) (16 patients) and control group (CG) (14 patients). SG was submitted of the PT treatment and participated of educative meetings, the CG only participated of the meetings. To evaluate adhesion to the AF was used the pedometer and EF was used a questionnaire of open and closed questions, six minute walk test (6'WT) and ergometric test (ET).
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 4
Kontakter og lokationer
Studiesteder
-
-
Goiás
-
Goiânia, Goiás, Brasilien, 75000000
- Liga de Hipertensão Arterial da Universidade Federal de Goiás
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- age or over 60 years,
- both sexes,
- regular frequency of hypertension league;
- practice of physical exercise irregular or absent (reported by professionals objectively on the record)and signature of informed consent. -
Exclusion Criteria:
- participate in another research project;
- refuse to sign the informed consent.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Aktiv komparator: Kontrolgruppe
|
This group only participed of education meeting (every fifteen days)
|
Eksperimentel: Studiegruppe
|
Physical therapy was realized three two times per week and education meeting every fifteen days
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
to verify if physical therapy (PT) treatment can improve the AF and EF adhesion of hypertensive aged
Tidsramme: nine months
|
nine months
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
To evaluate adhesion to the AF was used the pedometer and EF was used a questionnaire of open and closed questions, six minute walk test (6'WT) and ergometric test (ET)
Tidsramme: Nine months
|
Nine months
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Priscila Vitorino, MsD, Liga de Hipertensão Arterial da Universidade Federal de Goiás
- Studiestol: Paulo César Jardim, PhD, Liga de Hipertensão Arterial da Universidade Federal de Goiás
- Studiestol: Flávia Nogueira, Specialist, Liga de Hipertensão Arterial da Universidade Federal de Goiás
- Studiestol: Juliana Brandão, Specialist, Liga de Hipertensão Arterial da Universidade Federal de Goiás
- Studiestol: Haden Lobo, Specialist, Liga de Hipertensão Arterial da Universidade Federal de Goiás
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 1-Vitorino
- 0136/03
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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