Terminé

Comprehensive Approach for Hypertension Prevention and Control in Argentina

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Ce qui est testé

Comprehensive Intervention

Comportemental
Qui peut participer

Maladies Cardiovasculaires

+ Maladies vasculaires

+ Hypertension

À partir de 21 ans
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Étude thérapeutique

Interventionnel
Date de début : juin 2013
Voir le détail du protocole

Résumé

Sponsor principalTulane University
Dernière mise à jour : 17 juillet 2017
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Date de début de l'étude : 1 juin 2013

Date à laquelle le premier participant a commencé l'étude.

Background: Although the efficacy and effectiveness of lifestyle modifications and antihypertensive pharmaceutical treatment for the prevention and control of hypertension and concomitant cardiovascular disease and premature death have been demonstrated in randomized controlled trials, this scientific knowledge has not been fully applied in the general population, especially in low and middle income countries. Objectives: To test whether a comprehensive intervention program within a national public primary care system will improve hypertension control among uninsured hypertensive patients and their families in Argentina Design: Cluster randomized trial Study Participants: 1,890 study participants from 18 primary care clinics within a public primary care network in Argentina will be recruited. Patients with hypertension from the participating clinics, their spouses, and their adult hypertensive family members will be enrolled. Intervention: Nine clinics with approximately 945 participants will be randomly assigned to the comprehensive intervention group and 9 clinics with similar participants to the usual care group. The comprehensive intervention, including health care provider education, a home-based intervention among patients and their families (lifestyle modification and home blood pressure [BP] monitoring) delivered by community health workers, and a mobile health intervention, will last for 18 months. Outcomes: BP and other indicators will be measured at baseline and months 6, 12, and 18 during follow-up using standard methods. The primary outcome is a net change in systolic (SBP) and diastolic BP (DBP) from baseline to month 18 between the intervention and control groups among hypertensive study participants. The secondary outcomes are the proportion of hypertensive patients with adequate BP control (BP<140/90 mmHg), cost-effectiveness of hypertension control, and net BP changes in normotensive participants.

NCT01834131
Sponsor principalTulane University
Dernière mise à jour : 17 juillet 2017
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design

1954 participants à inclure

Nombre total de participants que l'essai clinique vise à recruter.

Traitement

Cette étude teste un ou plusieurs traitements pour évaluer leur efficacité contre une maladie ou un problème de santé spécifique. L'objectif est de voir si un nouveau médicament ou une thérapie fonctionne mieux, ou provoque moins d'effets secondaires que les options existantes.



Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Conditions
Critères

Tout sexe

Le sexe biologique des participants éligibles à s'inscrire.

À partir de 21 ans

Tranche d'âge des participants éligibles à participer.

Volontaires sains autorisés

Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.

Conditions

Pathologie

Maladies CardiovasculairesMaladies vasculairesHypertension

Critères

Inclusion Criteria for Clinics: The clinic is affiliated with the Remediar+Redes program. The clinic is located in urban poor areas according to the 2010 census data. The clinic has ≥1000 outpatient visits each month, so that sufficient participants can be recruited. The minimum distance between the selected clinics will be 10 kilometers to minimize the risk for contamination of the intervention. Physician visits and essential medications are free of charge to patients under all circumstances. The clinic has a high number of prescriptions for antihypertensive medications. The clinic employs community health workers. The clinic has general practitioners and nurses. The clinic has a history of good performance in the Remediar+Redes program. The clinic performs blood draws on patients when appropriate. Inclusion Criteria for Participants: Patients aged ≥21 years who received primary care from the participating clinics and have hypertension ( SBP ≥140 mmHg and/or DBP ≥90 mmHg on at least 2 separate visits) and their spouses (with or without hypertension) and/or any adult hypertensive family members (age ≥21 years) living in the same household will be included. Hypertension patients and their spouses and/or family members must be available for the first baseline nurse home visit. The index patient must have a cell phone that receives text messages. The family's homes must be located within 10 kilometers from the clinic. Exclusion Criteria for Participants: Hypertension patients who do not have a spouse or another adult with hypertension in the household. Plans to move from the neighborhood in the next two years Pregnant women or women who are planning to become pregnant in the next two years Persons who are bed-bound Persons who cannot give informed consent Persons with an arm circumference >50 cm

Plan de l'étude

Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.
Groupes de traitement
Objectifs de l'étude

2 groupes d'intervention sont désignés dans cette étude

Cette étude ne comporte pas de groupe placebo. 

Groupes de traitement

Groupe I

Pas d'intervention
Clinics assigned to usual care will not receive any of the intervention components. Physicians in these clinics will continue to treat patients using their usual methods. Participants from these clinics will not receive community health worker visits or the mobile health intervention

Groupe II

Expérimental
Physicians will receive training in the use of treatment algorithms based on hypertension guidelines. Community health workers (CHW) will be trained in facilitating behavioral change through BP monitoring, medication management, and lifestyle modifications. CHW will serve as a source of education, motivation, and social support, and as facilitators of healthcare utilization for participants. CHW will conduct home visits, schedule appointments with primary care physicians, deliver antihypertensive medications to patients' homes, and provide tailored counseling to address barriers to behavior change. Individualized text messages to promote lifestyle changes and reminders to reinforce medication adherence will be sent to participants weekly.

Objectifs de l'étude

Objectifs principaux

Objectifs secondaires

Centres d'étude

Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.

Cette étude comporte 1 site

Institute for Clinical Effectiveness and Health Policy

Buenos Aires, ArgentinaOuvrir Institute for Clinical Effectiveness and Health Policy dans Google Maps
Terminé1 Centres d'Étude