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Using Social Norms to Encourage People to Exercise More

15 settembre 2016 aggiornato da: Hengchen Dai, Washington University School of Medicine
The investigators are interested in using social norms to motivate people to sign up for a 100-day exercise challenge and exploring how to make social norms messages more effective.

Panoramica dello studio

Descrizione dettagliata

The investigators are interested in using social norms to motivate people to sign up for a 100-day exercise challenge and exploring how to make social norms messages more effective. Specifically, the primary purposes of this study are to test (a) whether social norms messages (i.e., information about how many people have signed up for the challenge) can increase signup rates and eventually lead people to exercise more and (b) whether such messages become more effective when they highlight different types of motivations (intrinsic vs. extrinsic motivations). Through a partnership with a university, the investigators are running a large-scale, randomized field controlled trial aimed at increasing sign-ups for the challenge and exercise frequencies during the challenge.

Benefits-eligible employees at the partner university are randomly assigned to one of four experimental conditions and receive the corresponding version of email message encouraging them to sign up for the challenge.

(1) In the control group, the email does not mention the number of people who have signed up. (2) In the norm condition, the email mentions the number of people who have signed up. (3) In the norm and health motive condition, the email mentions the number of people who have signed up, and highlights that the challenge is designed to help people to stay fit in a fun way. (4) In the norm and reward motive condition, the email mentions the number of people who have signed up, and highlights that the challenge is designed to help people to stay active and earn rewards.

The investigators hypothesize that Groups 2, 3, and 4 will have a higher sign-up rate and higher exercise frequencies on average than Group 1, because positive social norms should motivate people to engage in the target, desirable behavior. Also, the investigators will compare sign-up rates and exercise frequencies between Groups 2, 3, and 4 to examine whether highlighting intrinsic and extrinsic motives can further increase sign-up rates and overall exercise frequencies than only giving social norms information.

All benefits-eligible employees at the partner university for whom the Human Resource (HR) office has an email address on record receive invitation emails from HR. The invitation emails that contain the interventions are sent out one week AFTER the registration period has started, because HR needs to know how many people sign up in the first week and use this information to create a social norms message. Employees who sign up for the challenge during the first week of the registration period (i.e., prior to the implementation of the interventions) cannot be affected by the interventions. Thus, the investigators decide in advance that these employees will be excluded from analysis.

Employees will receive two emails that are sent eight days apart from each other. Thus, the investigators plan to examine both the sign-up rates within one week after each email goes out and the overall sign-up rates throughout the 50-day registration period.

The investigators plan to explore moderators based on (a) employees' demographics (age, gender, ethnicity, position), (b) employees' participation in previous challenges, and (c) employees' health condition and fitness level prior to the challenge (such as how actively they have been participating in other wellness activities, their health statistics).

Tipo di studio

Interventistico

Iscrizione (Anticipato)

15000

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

    • Missouri
      • St. Louis, Missouri, Stati Uniti, 63108
        • Hengchen Dai

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

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  • All benefits-eligible employees at partner university for whom the Human Resource office has an email address on record

Exclusion Criteria:

  • Employees who sign up for the challenge prior to the implementation of the interventions will NOT be included in the analysis.

(The interventions are implemented one week after the registration period has started. The partner university has to send invitation emails to all benefits-eligible employees with an email address on record, including those who already signed up. However, employees who already signed up cannot be affected by the interventions and thus will be excluded from the analysis.)

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: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: Group 1: Control
People receive emails encouraging them to sign up for the challenge. The email does not mention the number of people who have signed up.
Receive emails encouraging them to sign up
Sperimentale: Group 2: Norm
People receive emails encouraging them to sign up for the challenge. The email mentions the number of people who have signed up.
Receive emails encouraging them to sign up
Receive information about how many people have signed up
Sperimentale: Group 3: Norm and health motive
People receive emails encouraging them to sign up for the challenge. The email mentions the number of people who have signed up AND highlights that the challenge helps people to stay fit in a fun way.
Receive emails encouraging them to sign up
Receive information about how many people have signed up
Receive information about how the challenge helps people to stay fit in a fun way
Sperimentale: Group 4: Norm and reward motive
People receive emails encouraging them to sign up for the challenge. The email mentions the number of people who have signed up AND highlights that the challenge helps people to stay active and earn rewards.
Receive emails encouraging them to sign up
Receive information about how many people have signed up
Receive information about how the challenge helps people to stay active and earn rewards

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Percentage of people who sign up for the challenge
Lasso di tempo: During the registration period, 50 days
Whether or not each person signs up for the challenge during the registration period
During the registration period, 50 days
Activity level
Lasso di tempo: Through study completion, 100 days
Number of steps taken each day, as recorded in participants' online portal
Through study completion, 100 days

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Body Mass Index (BMI)
Lasso di tempo: Most recent BMI as entered by participant, an expected average of 2 months after study start
most recent BMI in pounds (weight) and inches (height) as entered by participant, an expected average of 2 months after study start. Obtaining the data is dependent on the ability to obtain the data from the online portal.
Most recent BMI as entered by participant, an expected average of 2 months after study start
cholesterol
Lasso di tempo: Most recent cholesterol as entered by participant, an expected average of 2 months after study start
Most recent total, low, and high cholesterol levels in mg/dl as entered by participant, an expected average of 2 months after study start. Obtaining the data is dependent on the ability to obtain the data from the online portal.
Most recent cholesterol as entered by participant, an expected average of 2 months after study start
blood pressure
Lasso di tempo: Most recent blood pressure as entered by participant, an expected average of 2 months after study start
Most recent systolic and diastolic levels in mmHg as entered by participant, an expected average of 2 months after study start. Obtaining the data is dependent on the ability to obtain the data from the online portal.
Most recent blood pressure as entered by participant, an expected average of 2 months after study start
stress
Lasso di tempo: Most recent stress as entered by participant, an expected average of 2 months after study start
Most recent self-reported stress level on a 1-5 scale (with 1 indicating "Relaxed" and 5 indicating "Highly Stressed") as entered by participant, an expected average of 2 months after study start. Obtaining the data is dependent on the ability to obtain the data from the online portal.
Most recent stress as entered by participant, an expected average of 2 months after study start
Email open and click rates
Lasso di tempo: Through study completion, 100 days
The rates at which people in each experimental condition read the invitation emails and click on links in the emails
Through study completion, 100 days

Collaboratori e investigatori

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

Investigatori

  • Investigatore principale: Hengchen Dai, Ph.D, Washington University School of Medicine

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 settembre 2016

Completamento primario (Anticipato)

1 dicembre 2016

Completamento dello studio (Anticipato)

1 gennaio 2017

Date di iscrizione allo studio

Primo inviato

3 settembre 2016

Primo inviato che soddisfa i criteri di controllo qualità

15 settembre 2016

Primo Inserito (Stima)

20 settembre 2016

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

20 settembre 2016

Ultimo aggiornamento inviato che soddisfa i criteri QC

15 settembre 2016

Ultimo verificato

1 settembre 2016

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 201608038

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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