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Evaluating Consumer m-Health Services for User Engagement and Health Promotion: An Organizational Field Experiment

27. Juli 2015 aktualisiert von: Yi-Chin Lin, Carnegie Mellon University

Introduction Chronic disease is prevalent and costly in the U.S. (Tu & Cohen, 2009). Poor eating habit is one factor that account for risk of chronic disease (Arsand, Varmedal, & Hartvigsen, 2007). Smartphone technology has been promising to improve preventive health outcomes. However, its great potential has not been widely applied to people's eating behaviors and its impact is unknown.

Professional and peer supports can improve health status (Elkjaer et al., 2010; Lorig et al., 1999; Perri, Sears, & Clark, 1993). However, the former is usually delivered didactically or passively with limited use of smartphones. There is also little evidence of the effect of peer support delivered by smartphones in the domain of healthy eating. This research aims to study what smartphone technology can do to upgrade professional and peer supports, and to evaluate the impact of these mobile-app enabled supports on people's behavior of healthy eating and user engagement.

Hypotheses

According to Social Cognitive Theory, we hypothesize the following:

  1. Mobile-enabled self-monitoring approach improves users' healthy eating behaviors through improved self-efficacy
  2. Professional support improves users' healthy eating behaviors through improved self-efficacy
  3. Peer support improves users' healthy eating behaviors through improved self-efficacy
  4. The amount of support is positively correlated with the change in behaviors and their determinants

Experiment Design The hypotheses will be examined bya 4-month randomized field experiment. 375 subjects will be recruited and assigned to one of the five arms to receive the corresponding tool for diet management at no cost.

Arm 1: a mobile App with both professional and peer support Arm 2: a mobile App with peer support only Arm 3: a mobile App with professional support only Arm 4: a mobile App without any support Arm 5: a non-mobile web App In addition to the App usage data, five surveys are conducted at baseline and the end of each month. Respondents will be compensated by $8 and a chance to win $200 for each completed survey.

Interventions

  1. All subjects receive the following interventions: an education package includes the importance of healthy eating, concept of MyPlate, personalized daily food plans; reminders throughout the study; goal setting capabilities;
  2. Self-monitoring provided by an Android App: a heuristic approach inspired by MyPlate to record their food consumption which allows users to record their meals by images and doesn't require estimations in cups and ounces; daily reports and trend reports
  3. Self-monitoring provided by the web App: a traditional approach to record their food consumption which requires estimations in cups and ounces, and no images are allowed; no daily reports and trend reports are provided
  4. Professional support provided by a registered dietitian via the Android App: the supports include the following:

    1. Reply to users' messages regarding healthy eating
    2. Provide meal-specific comments on subjects' meal consumptions: one meal per week
    3. Provide feedback on the subjects' consumption patterns: once per week
  5. Peer support provided by other subjects via the Android App: the App provides platforms for subjects who have the same interest to communicate to each other. The actions the subjects can do in the platforms include:

    1. Post images or texts related to healthy eating
    2. Share meals with their ratings
    3. Like/dislike others' posts
    4. Comment on others' posts e Create groups which allow subjects who have the same interest to join

Measurements

  1. Dependent Variables

    1. Eating behavior: a score of healthiness of a meal will be assigned by a dietitian. The scores obtained by the same subject along the experiment compose the subject's eating behavior
    2. Engaging behavior: this is measured by the number of meals recorded by the subject in a week. The numbers for the same subject along the experiment compose the subject's engaging behavior
  2. Independent Variables

    1. Level of peer support: this will be measured by a score representing the number of posts, likes, and comments received and given by a subject in a week
    2. Level of professional support: this will be measured by a score representing the number of messages or comments exchanged with the dietitian in a week
  3. Mediator Variables: self-efficacy, outcome expectation, and impediments will be measured by survey instruments

Data

  1. User Survey: characteristics and perceptions
  2. Mobile App: time, location, and contents of goal setting, meal entries, communications with professionals and peers
  3. Web App: contents of goal setting and meal entries

Analysis Confirmatory factor analysis and statistical modeling such as structural equation modeling and mixed models will be conducted to test our hypotheses.

Studienübersicht

Studientyp

Interventionell

Einschreibung (Tatsächlich)

425

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Pennsylvania
      • Pittsburgh, Pennsylvania, Vereinigte Staaten, 15213
        • Carnegie Mellon University

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • age at least 18 years
  • Android smartphone users
  • having internet accessibility on the smartphone during the study period

Exclusion Criteria:

  • currently participating in other similar programs
  • having specific medical conditions that require specialized diets

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Unterstützende Pflege
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Mobile: Professional and peer support
A mobile app that provides both professional support and peer support
Experimental: Mobile: Peer support
A mobile app that provides peer support, but not professional support
Experimental: Mobile: Professional Support
A mobile app that provides professional support, but no peer support
Aktiver Komparator: Mobile: No Support
A mobile app that provides neither peer support nor professional support
Aktiver Komparator: Web: No Support
A web app that provides neither peer support, nor professional support

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Healthy Eating Behavior
Zeitfenster: 4 months after signed up
This will be measured by a score representing the healthiness of each selected meal, evaluated by dietitians. Specifically, the score is composed of three sub-scores: 1) portion of fruits and vegetables (7-point Likert scale); 2) portion of the entire meal (7-point Likert scale); 3) evaluators confidence level (4-point Likert scale). One subject will get one score per week, and hence 16 scores in 4-months.
4 months after signed up
Engaging Behavior
Zeitfenster: 4 months after signed up
This will be measured by the number of records submitted by the subject via the assigned tool in a week. One subject will get one score per week, and hence 16 scores in 4-months.
4 months after signed up

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Yi-Chin Lin, MS, Carnegie Mellon University
  • Studienstuhl: Rema Padman, PhD, Carnegie Mellon University
  • Studienleiter: Julie Downs, PhD, Carnegie Mellon University
  • Studienleiter: Vibhanshu Abhishek, PhD, Carnegie Mellon University

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. März 2014

Primärer Abschluss (Tatsächlich)

1. Oktober 2014

Studienabschluss (Tatsächlich)

1. Oktober 2014

Studienanmeldedaten

Zuerst eingereicht

31. Juli 2014

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

31. Juli 2014

Zuerst gepostet (Schätzen)

1. August 2014

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

28. Juli 2015

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

27. Juli 2015

Zuletzt verifiziert

1. Juli 2015

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • HS14-249

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