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Eine Studie entspricht den Filterkriterien
Kartenansicht
Randomized Trial of Exercise Promotion in Primary Care (EPPC)
Die Details der klinischen Studie sind hauptsächlich auf Englisch verfügbar. Trial Radar KI kann jedoch helfen! Klicken Sie einfach auf 'Studie erklären', um die Informationen zur Studie in der ausgewählten Sprache anzuzeigen und zu besprechen.
Die klinische Studie NCT04445168 (EPPC) ist eine interventionsstudie zur Untersuchung von Prädiabetes, Diabetes, Sitzendes Verhalten und hat den Status aktiv, nicht rekrutierend. Die Studie startete am 31. August 2020 und soll 451 Teilnehmer aufnehmen. Durchgeführt von Kaiser Permanente ist der Abschluss für 31. Dezember 2025 geplant. Die Daten von ClinicalTrials.gov wurden zuletzt am 24. März 2025 aktualisiert.
Kurzbeschreibung
Millions of Americans have diabetes or prediabetes, for which regular physical activity can reduce risks of unfavorable outcomes of these conditions. This study will test the effects of an evidence-based intervention in the primary care setting on increasing physical activity among these individuals. If effective, it can be broadly implemented in primary care.
Offizieller Titel
Intervention Based in Primary Care to Increase Physical Activity Among Inactive Adults With Prediabetes and Diabetes
Erkrankungen
PrädiabetesDiabetesSitzendes VerhaltenWeitere Studien-IDs
- EPPC
- KPSC IRB#10106M
NCT-Nummer
Studienbeginn (tatsächlich)
2020-08-31
Zuletzt aktualisiert
2025-03-24
Studienende (vorauss.)
2025-12-31
Geplante Rekrutierung
451
Studientyp
Interventionsstudie
PHASE
Nicht zutreffend
Status
Aktiv, nicht rekrutierend
Stichwörter
Physical activity
Randomized trial
Primary care
Randomized trial
Primary care
Primäres Ziel
Prävention
Zuteilungsmethode
Randomisiert
Interventionsmodell
Parallel
Verblindung
Dreifach
Studienarme/Interventionen
| Teilnehmergruppe/Studienarm | Intervention/Behandlung |
|---|---|
Keine InterventionUsual Care Participants assigned to usual care may receive advice from their primary care physician to increase their physical activity. They will receive handouts about every 6 weeks on general health topics. | Nicht zutreffend |
ExperimentellIntervention Participants assigned to the intervention arm will receive telephone-based motivational interviews with trained interventionists to encourage increases in physical activity. | Telephone-based Motivational Interviews 2-year telephone-based motivational interviews to increase physical activity. |
Hauptergebnismessungen
Nebenergebnismessungen
| Ergebnismessung | Beschreibung der Messung | Zeitrahmen |
|---|---|---|
Moderate to vigorous physical activity (MVPA) | Accelerometer-derived 7-day MVPA | 12 months |
Moderate to vigorous physical activity (MVPA) | Accelerometer-derived 7-day MVPA | 24 months |
| Ergebnismessung | Beschreibung der Messung | Zeitrahmen |
|---|---|---|
Weight | Weight assessed from electronic medical records | 12 months |
Weight | Weight assessed from electronic medical records | 24 months |
Systolic blood pressure | Systolic blood pressure assessed from electronic medical records | 12 months |
Systolic blood pressure | Systolic blood pressure assessed from electronic medical records | 24 months |
Diastolic blood pressure | Diastolic blood pressure assessed from electronic medical records | 12 months |
Diastolic blood pressure | Diastolic blood pressure assessed from electronic medical records | 24 months |
HbA1c | HbA1c assessed from electronic medical records | 12 months |
HbA1c | HbA1c assessed from electronic medical records | 24 months |
Health-related quality of life | Assessed from the short form (SF-8) instrument; scale 0 - 100, higher is more favorable quality of life | 12 months |
Health-related quality of life | Assessed from the short form-8 instrument; scale 0 - 100, higher is more favorable quality of life | 24 months |
Eignungskriterien
Zugelassene Altersgruppen
Erwachsene, Ältere Erwachsene
Mindestalter
18 Years
Zugelassene Geschlechter
Alle
Able to speak English or Spanish, Inactive defined as less than 30 minutes of MVPA per week, Prediabetes or diabetes not prescribed insulin, Kaiser Permanente member for at least 12 months, Receives primary care at the Fontana Medical Center, Body mass index between 18.5 and 40 kg/m2,
Current use of insulin, Cardiovascular event in the past 6 months or other condition that limits physical activity, Pregnancy, breastfeeding or planning pregnancy in next 2 years, Current participation in another clinical trial or research study, Plans to move out of the area in next 2 years,
Kaiser PermanenteKeine Kontaktdaten vorhanden
1 Studienstandorte in 1 Ländern
California
Kaiser Permanente Southern California, Pasadena, California, 911010, United States