- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01129895
Promoting Health by Self Experience (PHASE) Randomized Controlled Trial (PHASE)
Promoting Health by Self Experience (PHASE) randomized controlled trial
Study Hypothesis:
A personal experience in health promotion will affect the health prevention activities of the health providers and thus will impact their prevention activities toward their patients compared with a control (no-intervention) group.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Objective: To evaluate the effectiveness of a personal experience and personal initiation program on the health prevention activities of the health providers and the following impact on their patients compared with a control (no-intervention) group.
Methods: A randomized controlled trial Randomization: Health providers of all disciplines will be recruited from 10 clinics of Clalit Health Services, Dan district and randomized using cluster (by clinic) randomization, into an intervention and a control group. In each clinic 15 health care providers and 50 patients will be interviewed providing a total of 150 health care providers and 500 patients.
Intervention: The intervention will be delivered by psychologists and social workers trained in group facilitation and experimental learning. The program is based on theories of experimental learning and Bridges model of change. In each intervention clinic 5 workshops on the initiation of health prevention projects in each clinic will be organized by the intervention team and than the clinic will be followed by the intervention team for 6 months. No intervention will be provided to the control clinics.
Outcomes: changes in quality measurements of both intervention and non-intervention clinics. Among health providers changes in attitudes, personal views and life style as well as health prevention activities will be assessed by questionnaires. A random sample of 50 patients age 21-50 from each of the participating clinics will be selected and interviewed using a questionnaire. The questionnaires will include questions regarding the administration of screening tests, treatment of abnormal measurements, life style changes and satisfaction with the performance of the clinic and health care providers. The evaluation for both health care providers and patients will be performed at baseline and after 6 months.
Tipo di studio
Iscrizione (Anticipato)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
-
-
-
Petach Tikva, Israele
- Reclutamento
- Clalit Health Services
-
Contatto:
- Dorit Erlich, MD
- Numero di telefono: 972507348786
- Email: dorite@clalit.org.il
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Health providers in selected clinics
- Patients age 21-50 in selected clinics
Exclusion Criteria:
- Patients age younger than 21 and older than 50
- Health providers from clinics not in the area of the study
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
---|---|
Sperimentale: Health promotion
5 workshops on the initiation of health prevention projects in each clinic will be organized by the intervention team and than the clinic will be followed by the intervention team for 6 months.
|
In each intervention clinic 5 workshops on the initiation of health prevention projects in each clinic will be organized by the intervention team and than the clinic will be followed by the intervention team for 6 months.
|
Nessun intervento: Promoting Health
No intervention follow-up only
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Promoting Health randomized controlled trial
Lasso di tempo: 6 months
|
Changes in quality measurements Changes in attitudes, personal views and life style as well as health prevention activities
|
6 months
|
Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Iris Shai, PhD, Ben-Gurion University of the Negev
- Investigatore principale: Danit R Shahar, PhD, Ben-Gurion University of the Negev
Pubblicazioni e link utili
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Anticipato)
Completamento dello studio (Anticipato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Altri numeri di identificazione dello studio
- unilever-0410-OL
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 .
Prove cliniche su Health promotion
-
IWK Health CentreNon ancora reclutamento
-
Radicle ScienceAttivo, non reclutanteDolore addominale | Digestione | Disturbi gastrointestinaliStati Uniti
-
Boston UniversityEunice Kennedy Shriver National Institute of Child Health and Human Development... e altri collaboratoriReclutamentoAllattamento al seno | SUID | SIDStati Uniti
-
Boston Children's HospitalUnited States Department of Defense; National Football LeagueCompletato
-
Manan ShuklaCompletato
-
Hacettepe UniversityCompletatoDiabete di tipo 2Tacchino
-
Philips Electronics Nederland B.V. acting through...Medisch Spectrum TwenteReclutamento
-
Noctrix Health, Inc.CompletatoSindrome delle gambe agitateStati Uniti
-
Radicle ScienceCompletatoDepressione | Dolore | Sonno | AnsiaStati Uniti
-
The University of Hong KongNon ancora reclutamentoPredisposizione genetica alla malattia | Malattia coronarica | Tempo sedentario | Tracker per il fitness