Fit Physicians: Use of Activity Monitors and Activity Integration Program in First Year Medical Students (FitPhysician)
Fit Physicians: A Novel Physical Activity Integration Program to Improve Fitness and Activity in Medical Students: A Randomized Pilot Study
Studieoversikt
Status
Intervensjon / Behandling
Detaljert beskrivelse
Using fitness trackers and exercise testing, it will determine if participating in a novel program that incorporates wellness into the academic term will improve fitness.
An estimate, 120 students will enroll in this study. Men and women aged 18-55 years of age that are just entering medical school. Students who are currently pregnant will not be allowed to participate in this study.
Participation will involve 2 visits at the start of the academic school year, and two visits at the end of the academic school year.
These visits will entail you undergoing a body composition scan measured by an duel energy x-ray absorptiometry (iDEXA) machine. The scan takes approximately 15 minutes. Subjects may be asked to perform an exercise stress test on a treadmill. The exercise test is approximately 40 minutes. Subjects may be asked to participate in a fitness program 2x a week, and may be asked to wear a Fitbit Flex™ activity tracker on the wrist for the duration of the school year. Investigators will be accessing academic grades to use for statistical purposes only. Subject names will never be given to any other party other than the investigators involved.
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
New York
-
Old Westbury, New York, Forente stater, 11568568
- NYIT
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- First year medical students
- Must have smartphone
Exclusion Criteria:
- Medical conditions that prohibit exercise
- pregnancy
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Annen
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Fit Physician Group
Subjects will receive activity monitor and will be required to attend monthly wellness lectures and weekly exercise intervention. Every subject will undergo an iDEXA scan to measure body mass composition |
Subjects will receive pre study and post study scans to assess body mass composition
Subjects in the Fit Physician Arm will be required to attend monthly wellness lectures
Subjects in the Fit Physician Arm will be required to attend weekly exercise interventions
Subjects in the Fit physician arm and the activity monitor arm will receive activity monitors to assess their activity level throughout the academic year
|
|
Aktiv komparator: Activity Monitor Only Group
Subjects will receive an activity monitor without any intervention Every subject will undergo an iDEXA scan to measure body mass composition ) |
Subjects will receive pre study and post study scans to assess body mass composition
Subjects in the Fit physician arm and the activity monitor arm will receive activity monitors to assess their activity level throughout the academic year
|
|
Annen: Control Group
Subjects will not an activity monitor nor will they receive any intervention Every subject will undergo an iDEXA scan to measure body mass composition
|
Subjects will receive pre study and post study scans to assess body mass composition
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Steps per day measured daily by FitBit Flex
Tidsramme: 10 months
|
10 months
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Body Mass Composition assessed by iDEXA scan
Tidsramme: 10 months
|
10 months
|
|
Academic Performance assessed by numeric grade point average
Tidsramme: 10 months
|
10 months
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Studiestol: Brian Harper, MD, NYIT College of Osteopathic Medicine
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- BHS-1153
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .