- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT02496728
NUYou:mHealth Intervention to Preserve and Promote Ideal Cardiovascular Health (NUYou)
American Heart Association Strategically Focused Research Network: mHealth Intervention to Preserve and Promote Ideal Cardiovascular Health
Studienübersicht
Status
Bedingungen
Detaillierte Beschreibung
Freshman college students at Northwestern University will be cluster randomized to two groups based on their dorm. The intervention for one group will target smoking, physical activity, BMI and consumption of fruits and vegetables. The intervention in the second group will target traveling behavior, sexual risk behaviors, sunscreen use and hydration. Baseline health and lifestyle measures will be assessed for each participant prior to intervention. Health assessments will measure height, weight, fasting glucose, total cholesterol and carbon monoxide. The lifestyle measure will ask questions about physical activity, diet, alcohol and tobacco use, safe sex practices, driving habits, and sunscreen use. These same measures will be repeated during the fall of the students' sophomore and junior years.
Participants will be given a mobile application and encouraged to track some behaviors. In addition, participants will be asked to answer weekly questions regarding health behaviors.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Illinois
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Chicago, Illinois, Vereinigte Staaten, 60611
- Northwestern University
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-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Freshman at Northwestern University in the fall of 2015
- Live on campus
- Read, write and speak English
- Own an Iphone or Android smart phone
Exclusion Criteria:
- Pregnant or trying to become pregnant
- Established cardiovascular disease
- Unstable psychiatric or medical condition
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Cardiovascular Health
Participants will be given the results of their health assessment and feedback regarding their health behaviors and overall health.
Recommendations for change will be given if warranted.
Participants will download the study's mobile health application on their smartphone.
They will then be asked to report once a week about their health behaviors on the application.
Participants will also be asked to self-monitor health behaviors that are not already at ideal levels using the study application (environmental cues).
Participants will be asked to join a secret Facebook group where informational materials will be posted, participants can post about study health behaviors and social interaction around health behaviors can occur (social support and environmental cues).
|
An application on a smart phone that is designed to help individuals self-monitor health behaviors.
Text messages, informational posts and reminders supporting healthy behaviors.
Participants may interact with each other through a private Facebook group.
Educational materials regarding healthy behaviors.
|
|
Aktiver Komparator: Whole Health
Participants will be given the results of their health assessment.
They will then receive educational materials about sunscreen use, safe sex, hydration and vehicular safety.
Participants will download the study's mobile health application on their smartphone.
They will then be asked to report once a week about their health behaviors on the application.
Participants will also be asked to self-monitor how much water they drink using the study application.
Participants will be asked to join a secret Facebook group where informational materials will be posted, they can post about study health behaviors and social interaction around health behaviors can occur (social support and environmental cues).
|
An application on a smart phone that is designed to help individuals self-monitor health behaviors.
Text messages, informational posts and reminders supporting healthy behaviors.
Participants may interact with each other through a private Facebook group.
Educational materials regarding healthy behaviors.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
American Heart Association MyLifeCheck (Simple 7) score as a measure of cardiovascular health
Zeitfenster: 2 years
|
Participant's Simple 7 score is the sum of 7 cardiovascular health metrics attained at ideal levels as defined by American Heart Association.
1) physically active - Exercising at least 150 minutes of moderate or 75 minutes of vigorous physical activity per week.
2) Good diet quality - Eating 5 servings of fruits and vegetables per day, at least 3 servings of whole grain, and no more than 16 oz. of soda per day, rarely or never eats high sodium foods or processed meats.
3) nonsmoking - nonsmoker for at least a year.
4) not overweight - BMI < 25 kg/m2.
5) normoglycemic - fasting glucose < 100 mg/dl.
6) not hypercholesterolemic : total Cholesterol < 200 mg/dl.
7) not hypertensive.
Blood Pressure <120/<80.
|
2 years
|
Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Publikationen und hilfreiche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 14SFRN20480260
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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