- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02019953
Effects of Health Promoting Programs on Cardiovascular Disease Risk
Effects of Health-Promoting Programs on Cardiovascular Disease Risk: JHS
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
The project is designed to achieve five specific aims: (1) To determine the feasibility of attracting African Americans into Health Promotion Research studies;(2) To determine whether clinically recorded information can be used as a guide for recruitment inclusion in Health Promotion Studies from an active epidemiological research cohort;(3) To measure the ability to retain African Americans recruited into Health Promotion Studies from an active research cohort;(4) To measure the adherence to various protocols within a Health promotion Study; and(5) To provide informed estimates of effect sizes for designing future Health Promotion Research.
A total of 375 study participants from the Jackson Heart Study (JHS) cohort, all of whom are African American, will be randomly assigned to one of five, equally-sized study arms: (1) practicing yoga three times per week; (2) practicing yoga two times per week; (3) practicing yoga one time per week; (4) walking briskly three times per week; and (5) attending a weekly healthy lifestyles class.
All study arms will include a 24-week intervention. In addition, participants will have a total of four clinical visits with members of the study team baseline, 12 weeks, 24 weeks, and 48 weeks) in which the following measures will be recorded:
- Systolic and diastolic blood pressure and heart rates
- Highly sensitive C-reactive protein (hsCRP) - serum, fibrinogen - plasma (sodium citrate), homocysteine (plasma), and interleukin-6 levels (IL-6) (serum).
- Fasting total cholesterol, low density (LDL), direct high density lipoprotein (HDL), and triglyceride levels - all serum
- HbA1c level
- BMI, waist circumference
- Medication and supplement use and dosages
- Results of a study survey designed to measure participants' changes in their reported health-related quality of life, perceived stress, health behaviors, sleep patterns, and impact of pain on everyday life
In addition, we will also record systolic and diastolic blood pressure and heart rates before and after each intervention session for all five study arms.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
-
-
Mississippi
-
Jackson, Mississippi, États-Unis, 39216
- University of Mississippi Medical Center
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- This study includes only one inclusion criterion: to participate in this study, one needs to be a member of the Jackson Heart Study cohort.
Exclusion Criteria:
1. Newly diagnosed (within the last six weeks) with a myocardial infarction, cerebrovascular disease, atrial fibrillation, cardiomyopathy, valvular heart disease, fatal cardiac arrhythmia, severe systolic and diastolic heart failure, uncontrolled COPD, uncontrolled moderate to severe hypertension, or a recent recipient of a pacemaker, and/or
2. Change in blood pressure medicine or lipid-lowering medication up to 30 days prior to or plans for a change in the 30 days after enrollment in the study, and/or
3. Already practicing yoga at least once per week or walking briskly for one hour at least three times per week, and/or
4. Inability to attend protocol sessions, and/or
5. Diagnosis of an underlying medical illness that might be considered by the principal investigator to potentially impair one's safety or ability to complete the study protocol (example could possibly include uncontrolled asthma), and/or
6. Current use of a prescription regimen that might be considered by the principal investigator to potentially impair one's safety or ability to complete the study protocol (examples could possibly include use of sedatives or other drugs that could affect a participant's ability to participate in any of the study arms).
7. Pregnant or planning to become pregnant in the next six (6) months.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Autre
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
---|---|
Autre: Yoga 3 times per week
Yoga participation 3 x per week for 24 weeks; 48 week follow-up.
|
The yoga intervention, which is taught based on Hatha yoga, will be offered to study participants in Study Arms 1, 2, and 3, is a combination of asanas (poses), pranayams (breathing exercises), and meditation.
Blood pressure and heart rate measurements are taken before and after each session.
|
Autre: Yoga 2 times per week
Yoga participation 2 x per week for 24 weeks; 48 week follow-up
|
The yoga intervention, which is taught based on Hatha yoga, will be offered to study participants in Study Arms 1, 2, and 3, is a combination of asanas (poses), pranayams (breathing exercises), and meditation.
Blood pressure and heart rate measurements are taken before and after each session.
|
Autre: Yoga 1 time per week
Yoga participation 1 x per week for 24 weeks; 48 week follow-up
|
The yoga intervention, which is taught based on Hatha yoga, will be offered to study participants in Study Arms 1, 2, and 3, is a combination of asanas (poses), pranayams (breathing exercises), and meditation.
Blood pressure and heart rate measurements are taken before and after each session.
|
Autre: Walking 3 times per week
Walking 3x per week for 24 weeks; 48 week follow-up
|
The walking intervention, which is Study Arm 4 includes, three guided walking sessions per week for 24 weeks.
Each class is an hour in length and will include a minimum of 30 minutes of walking at the equivalent of a minimum of three miles per hour.
Each session includes a ten-minute warm-up and ten-minute cool-down period of some stretches and walking at a leisurely pace.
Blood pressure and heart rate measurements are taken before and after each session.
|
Autre: Healthy Lifestyles Education
Healthy Lifestyles Education Participation 1 x per week for 24 weeks; 48 week follow-up
|
Participants randomly assigned to the fifth study arm attend one 60-minute healthy lifestyles class per week for 24 weeks.
The Healthy Lifestyles curriculum includes 24 independent lesson modules, which allows participants to begin their intervention at any time during the course schedule.
Blood pressure and heart rate measurements are taken before and after each session.
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Primary outcomes for this feasibility study will focus on composite measures for recruitment, retention, and the reasons for refusal or dropout.
Délai: Bi-annual for up to 52 weeks after enrollment
|
Primary outcomes for this feasibility study will focus on measures for recruitment, retention, and the reasons for refusal or dropout, and consist of (1) agreement to participate in the study (recruitment); (2) reasons for participating/not-participating; (3) dropout, defined as a monotone missingness pattern of stopping participation before completion of the study; (4) reasons for discontinuation/dropout; (5) attendance, defined as the potentially non-monotone pattern of coming to the scheduled study session; and (6) adherence, defined as attending and completing the scheduled sessions and clinical visits.
|
Bi-annual for up to 52 weeks after enrollment
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Changes in participants' hypertension profiles.
Délai: 48 weeks
|
Defined using measures of their systolic and diastolic blood pressure
|
48 weeks
|
Changes in participants' inflammation markers
Délai: 48 weeks
|
Defined using measures of participants' hsCRP, fibrinogen, homocysteine, and interleukin-6 levels.
|
48 weeks
|
Changes in participants' lipids profiles.
Délai: 48 weeks
|
Defined as using measures of participants' fasting total cholesterol, LDL, HDL, and triglycerides.
|
48 weeks
|
Changes in participants' HbA1c levels.
Délai: 48 weeks
|
Changes in participants' HbA1c levels.
|
48 weeks
|
Changes in participants' reported health-related quality of life.
Délai: 48 weeks
|
Quality of life measured as measured by perceived stress, health behaviors, sleep patterns, and impact of pain on everyday life.
|
48 weeks
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Gailen D Marshall, MD, PhD, University of Mississippi Medical Center
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 2010-0057
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
Essais cliniques sur Yoga
-
University of Texas at AustinComplété
-
Universität Duisburg-EssenComplété
-
NMP Medical Research InstituteWarwick Research Services; Yog-KulamComplété
-
Northwestern UniversityComplété
-
University of MinnesotaComplété
-
Manhattan Physical Medicine and Rehabilitation,...New York UniversityComplété
-
Adiyaman University Research HospitalComplétéLa dépression | Stresser | Anxiété | Résilience psychologiqueTurquie
-
University of MinnesotaThe John A. Hartford Foundation; St. Catherine University; Midwest Nursing Center...ComplétéQualité de vie | Arthrose, Genou | Sommeil de mauvaise qualité | Déficience physiqueÉtats-Unis
-
NMP Medical Research InstituteYog-Kulam; Department of Zoology, University of Rajasthan, IndiaComplétéCéphalée chronique de type tensionInde
-
Johns Hopkins UniversityRetiréLa dépression | Hypertension oculaire | Stresser | Anxiété | Trouble du sommeilÉtats-Unis