- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01250392
The Effect of Active Choice on Nurse Visit Participation
The Effect of Time-Slot Scheduling and Active Choice on Biometric Screening and Nurse Visit Participation
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
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Nevada
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Las Vegas, Nevada, Vereinigte Staaten, 89119
- Caesars Corporate Office
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Harrah's employee
- Registered e-mail address with Harrah's
- Part of Harrah's Choosing Wellness Program
Exclusion Criteria:
- Under 18
- Already participated in a nurse visit
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Versorgungsforschung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Sonstiges: Control Arm
The control group will be informed via e-mail of the window of dates during which they can take part in the on-site screening and given instructions for scheduling an appointment.
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The goal of this project is to see if active choice will increase an individual's likelihood of participating in a nurse visit. The employees in our sample will schedule their nurse visit time slot via e-mail and a health service provider website. The control group will be informed via e-mail of the window of dates during which they can take part in the on-site screening and given instructions for scheduling an appointment. The treatment group, the active choice only arm, will be given the same information as the control group, but they will also be asked to make an appointment immediately, defer the scheduling decision, or decline to receive a screening. The treatment group will also receive email reminders one week before their appointment.
Andere Namen:
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Experimental: Active Choice Only Arm
The active choice only arm, will be given the same information as the control group, but they will also be asked to make an appointment immediately, defer the scheduling decision, or decline to receive a screening.
|
The goal of this project is to see if active choice will increase an individual's likelihood of participating in a nurse visit. The employees in our sample will schedule their nurse visit time slot via e-mail and a health service provider website. The control group will be informed via e-mail of the window of dates during which they can take part in the on-site screening and given instructions for scheduling an appointment. The treatment group, the active choice only arm, will be given the same information as the control group, but they will also be asked to make an appointment immediately, defer the scheduling decision, or decline to receive a screening. The treatment group will also receive email reminders one week before their appointment.
Andere Namen:
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Nurse Visit Participation
Zeitfenster: This will be measured after all of the nurse visit windows have been closed, by 4/30/11
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We will measure whether or not subjects scheduled and participated in a nurse visit.
We will compare the number of subjects who participated in the nurse visits by treatment arms.
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This will be measured after all of the nurse visit windows have been closed, by 4/30/11
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Mitarbeiter und Ermittler
Mitarbeiter
Ermittler
- Hauptermittler: David I Laibson, Ph.D, National Bureau of Economic Research
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 (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Andere Studien-ID-Nummern
- 0001 (Researcher)
- P30AG034532 (US NIH Stipendium/Vertrag)
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