- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01262066
Effects of Lifeskills Workshop on BP in Hypertensive Employees (Lifeskills BP)
28. juli 2016 oppdatert av: National Heart, Lung, and Blood Institute (NHLBI)
RCT of LifeSkills Workshop on BP in Hypertensive Employees
A number of psychosocial risk factors have been strongly related to a range of health problems (chief among them CVD).
Clinical research has shown that behavioral interventions have enormous promise to ameliorate the psychosocial distress, the health-damaging effects and the costs associated with these risk factors.
However, few such programs have been implemented in a large-scale way.
Corporations are increasingly interested in providing such services for their employees, but they have encountered difficulties in knowing which programs are most effective.
Until these programs are developed as products that can be tested and shown to produce consistent benefits, dissemination of these beneficial programs will be hindered.
Taken together, these findings make a strong case that the development of a standardized, protocol-driven behavioral intervention package that can be delivered in a wide range of corporate settings presents a remarkable commercial opportunity.
The overall goal of this SBIR Fast-Track-funded project is to gain empirical evidence in a RCT that documents the effectiveness of the Williams LifeSkills Workshop (a protocol driven 6-session workshop) in reducing BP, psychosocial risk factors, and promoting positive health outcomes in a cost effective manner in a corporate setting.
This empirical support, tested in a setting independent of the program developers and by an experienced research team, will then be used to help market the product in the corporate wellness marketplace.
It is hypothesized that participants (employees in an urban medical center) in the LifeSkills intervention will experience greater reductions in blood pressure and improvements in measures of psychosocial well-being than those receiving usual medical care and given educational materials on reducing BP.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
181
Fase
- Fase 2
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år til 75 år (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Adults age 18-75
- Employees of Columbia University Medical Center
- BP >= 140/90 on 2 occasions (average of 3 readings each time)
Exclusion Criteria:
- Pregnancy
- End-stage Renal disease
- BP > 165/110 (average over 3 readings)
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Eksperimentell: LifeSkills workshop intervention
Participants attended 10 1-hr weekly sessions.
The content of the groups followed the LifeSkills Workshop manual and Video(Williams LifeSkills, Inc, Durham NC).
The LifeSkills Workshop is a structured psycho-educational group intervention using workbooks and videotapes that draw on cognitive-behavioral techniques and stress reduction approaches.
|
Intervention participants attended 10 one-hour weekly group sessions.
The content of the groups followed the LifeSkills Workshop manual and Video ( (Williams LifeSkills, Inc, Durham NC).
The LifeSkills Workshop is a structured psycho-educational group intervention using workbooks and videotapes that draw on cognitive-behavioral techniques and stress reduction approaches.
|
Ingen inngripen: Enhanced usual care
The Usual Care group received a self-help brochure on BP control developed by the National Heart, Lung, and Blood Institute (NHLBI).
In addition, with the participants' permission, their BP readings were sent to their listed physicians, along with the 1-page JNC-7 express summary for the management of high BP.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
change in mean office BP, covarying hostility and hostility x time (stratification variable)
Tidsramme: 2 months after end of treatment
|
The change in the mean office BP (evaluated automatically by BP-Tru device) from baseline to follow-up.
Hostility, evaluated by Cook-Medley questionnaire (Barefoot scoring) was a stratification variable and thus was used as a covariate in the analysis
|
2 months after end of treatment
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
Changes in mean office BP, controlling for baseline medications and medication changes during trial
Tidsramme: baseline to follow-up 2 months after end of intervention
|
baseline to follow-up 2 months after end of intervention
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Etterforskere
- Hovedetterforsker: Lynn P Clemow, PhD, Columbia University
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. september 2002
Primær fullføring (Faktiske)
1. august 2006
Studiet fullført (Faktiske)
1. august 2006
Datoer for studieregistrering
Først innsendt
15. desember 2010
Først innsendt som oppfylte QC-kriteriene
15. desember 2010
Først lagt ut (Anslag)
17. desember 2010
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
29. juli 2016
Siste oppdatering sendt inn som oppfylte QC-kriteriene
28. juli 2016
Sist bekreftet
1. november 2010
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- Lifeskills BP study
- R44HL067584 (U.S. NIH-stipend/kontrakt)
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. .
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