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

27 luglio 2015 aggiornato da: 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.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Effettivo)

425

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Pennsylvania
      • Pittsburgh, Pennsylvania, Stati Uniti, 15213
        • Carnegie Mellon University

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Terapia di supporto
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Mobile: Professional and peer support
A mobile app that provides both professional support and peer support
Sperimentale: Mobile: Peer support
A mobile app that provides peer support, but not professional support
Sperimentale: Mobile: Professional Support
A mobile app that provides professional support, but no peer support
Comparatore attivo: Mobile: No Support
A mobile app that provides neither peer support nor professional support
Comparatore attivo: Web: No Support
A web app that provides neither peer support, nor professional support

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Healthy Eating Behavior
Lasso di tempo: 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
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Yi-Chin Lin, MS, Carnegie Mellon University
  • Cattedra di studio: Rema Padman, PhD, Carnegie Mellon University
  • Direttore dello studio: Julie Downs, PhD, Carnegie Mellon University
  • Direttore dello studio: Vibhanshu Abhishek, PhD, Carnegie Mellon University

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 marzo 2014

Completamento primario (Effettivo)

1 ottobre 2014

Completamento dello studio (Effettivo)

1 ottobre 2014

Date di iscrizione allo studio

Primo inviato

31 luglio 2014

Primo inviato che soddisfa i criteri di controllo qualità

31 luglio 2014

Primo Inserito (Stima)

1 agosto 2014

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

28 luglio 2015

Ultimo aggiornamento inviato che soddisfa i criteri QC

27 luglio 2015

Ultimo verificato

1 luglio 2015

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • HS14-249

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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