Behavioral Study to Control Blood Pressure
Effect of a Novel Behavioral Intervention on Blood Pressure Control in Hypertension Patients
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Descrizione dettagliata
According to the National Health and Nutrition Examination Survey, more than 31% of adults in the U.S. population have hypertension (HTN). HTN is a major risk factor for heart disease and stroke, which are the 1st and 3rd leading causes of death in the U.S. and impose an enormous financial and social burden on Americans with more than $352 billion spent in direct and indirect costs. Behavioral interventions to control blood pressure (BP) have exhibited, on average, positive but relatively modest effects on blood pressure control. We and others have studied the effects of one such intervention - home BP monitoring - on BP control in hypertensive patients, and found reliable, albeit modest effects. We have found similar effects for another behavioral intervention, Motivational Interviewing, on BP control. We hypothesize that the effects of such interventions will be augmented when accompanied by a systematic approach to patient education concerning their illness and its treatment. The literature suggests that patient education is "necessary but not sufficient"(an implicit interaction) to produce behavioral changes; however, the "necessary" part tends to be ignored by interventionalists. The implication of the interaction is that when patients lack the necessary knowledge, any intervention is likely to be less effective (as any value multiplied by zero - i.e., no knowledge - is zero). In spite of this, we have found no trials that have tested the interaction between patient knowledge and a lifestyle or drug intervention.
We propose to test an intervention to increase patients' understanding of the causes, consequences, and the rationale for treatment, of their HTN, as a strategy for increasing BP control. The focus is on the interaction between a behavioral intervention to reduce BP - home BP monitoring (HBPM) - and patient knowledge, which, we propose, moderates the effect of the HBPM intervention. We hypothesize that patients who have a better understanding of their illness and its prescribed treatment will be more adherent to the treatment regimen, and thus will exhibit improved outcomes compared to those who have been exposed to the same intervention, but who do not have a clear understanding of these elements.
We propose to pilot test the effect of the HBPM intervention using a 2 X 2 independent groups randomized design, to allow us to compare the effects of Usual Care (UC) + Printed Materials (PM) compared to Usual Care (UC) and Self-Paced Programmed Instruction (SPPI) compared to Home Blood Pressure Monitoring (HBPM) + Printed Materials (PM) compared to Home Blood Pressure Monitoring (HBPM) + Self-Paced Programmed Instruction (SPPI).
Our primary hypothesis is:
Decreased ABP at 3 months will be ordered thusly:
HBPM+SPPI > HBPM+PM > UC+SPPI > UC+PM
Tipo di studio
Tipo di studio
Iscrizione (Effettivo)
Iscrizione
Fase
Fase
- Fase 2
- Fase 3
Contatti e Sedi
Luoghi di studio
-
-
Pennsylvania
-
Hershey, Pennsylvania, Stati Uniti, 17033
- Penn State Hershey Medical Center
-
-
Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- English speaking
- Has been diagnosed by physician has having hypertension/high blood pressure
- Has been prescribed medications to treat hypertension
- Has a blood pressure reading at the Screening Visit of either above 140/90
- If previously diagnosed with cancer, must be in remission
- Not currently pregnant or trying to become pregnant within next three months
- No major kidney, heart, liver failure
- Ages 21-80
- Must be able to travel to Hershey Medical Center (Hershey, PA)
Exclusion Criteria:
- Cannot read and speak English fluently
- Has not been diagnosed with hypertension
- Is not currently taking medications for hypertension
- Has blood pressure that is below 140 and 90
- Has blood pressure that is above 180 or 120
- Has cancer that is not in remission
- Is currently pregnant of plans to become pregnant in the next 3 months
- Has had major kidney, heart or liver failure
- Is less than 21 or greater than 80 years old
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Separare
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
|---|---|
|
Comparatore attivo: Usual Care (UC) + Printed Materials (PM)
If the participant is assigned to UC, they will receive standard care.
They will not receive a HBPM to use for the study, but will be given one to keep at the 3 month Follow-Up Visit.
If they are also assigned to PM, they will then be given written materials (pamphlets from the NIH) and will be asked to review the information in its entirety.
The coordinator will be available to answer any questions they might have.
|
Cura standard
National Institutes of Health Printed Materials on hypertension
Altri nomi:
|
|
Sperimentale: UC + Self-Paced Program Instruction (SPPI)
If the participant is assigned to UC, they will receive standard care.
They will not receive a HBPM to use for the study, but will be given one to keep at the 3 month Follow-Up Visit.
If they are also assigned to SPPI, they will be asked to complete a series of educational modules at their own pace on the laptop that is provided.
They will be informed that there is no grading and that the program is set up so that they can go at their own pace.
The SPPI modules will be designed directly from the information provided on the Printed Materials from the National Institutes of Health.
|
Cura standard
If participants are assigned to SPPI, they will be asked to complete a series of educational modules at their own pace on the laptop that is provided.
They will be informed that there is no grading and that the program is set up so that they can go at their own pace.
The SPPI modules will be designed directly from the information provided on the Printed Materials (PM) from the National Institutes of Health.
|
|
Sperimentale: Home Blood Pressure Monitor (HBPM) + PM
If the participant is assigned to HBPM, they will be asked to use the monitor once a day in the morning and once before they go to bed any 3 days of the week, each week of the study (total = 12 weeks).
They will be asked to record their BP values in diaries they will be given to take home with them.
If they are also assigned to PM, they will then be given written materials (pamphlets from the NIH) regarding hypertension education and will be asked to review the information in its entirety.
The coordinator will be available to answer any questions they might have.
|
National Institutes of Health Printed Materials on hypertension
Altri nomi:
The home blood pressure monitor will allow the participant to measure their blood pressure anytime and anywhere precisely, quickly and easily on their upper arm.
Altri nomi:
|
|
Sperimentale: HBPM + SPPI
If the participant is assigned to HBPM, they will be asked to use the monitor once a day in the morning and once before they go to bed any 3 days of the week, each week of the study (total = 12 weeks). They will be asked to record their BP values in diaries they will be given to take home with them. If they are also assigned to SPPI, they will be asked to complete a series of educational modules at their own pace on the laptop that is provided. They will be informed that there is no grading and that the program is set up so that they can go at their own pace. The SPPI modules will be designed directly from the information provided on the PM from the National Institutes of Health. |
If participants are assigned to SPPI, they will be asked to complete a series of educational modules at their own pace on the laptop that is provided.
They will be informed that there is no grading and that the program is set up so that they can go at their own pace.
The SPPI modules will be designed directly from the information provided on the Printed Materials (PM) from the National Institutes of Health.
The home blood pressure monitor will allow the participant to measure their blood pressure anytime and anywhere precisely, quickly and easily on their upper arm.
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Decreased Arterial Blood Pressure
Lasso di tempo: 3 months
|
3 months
|
Collaboratori e investigatori
Sponsor
Sponsor
Collaboratori
Collaboratori
Investigatori
Investigatori
- Investigatore principale: Christopher Sciamanna, MD, MPH, Milton S. Hershey Medical Center
Studiare le date dei record
Studia le date principali
Inizio studio
Inizio studio
Completamento primario (Effettivo)
Completamento primario
Completamento dello studio (Effettivo)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- 687
- R01HL089402-01A2 (Sovvenzione/contratto NIH degli Stati Uniti)
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 Solita cura
-
NCT05219357Attivo, non reclutanteDisturbo psichiatrico
-
NCT07170007ReclutamentoEpisiotomia | Lesione perineale | Dolore perineale | Strappo perineale derivante dal parto | Lacerazioni perineali | Lesione ostetrica dello sfintere anale | Strappo perineale ed episiotomia | Lacerazione, strappo o rottura perineale durante il parto
-
NCT04831697Completato
-
NCT01474057CompletatoDisturbo post-traumatico da stress (PTSD)
-
NCT06618755ReclutamentoDipendenza | Disturbo da uso di alcol | Ricaduta | Astinenza da alcol | Colloqui motivazionali
-
NCT05825820Non ancora reclutamentoIdeazione suicida | Suicidio, tentato | Suicidio
-
NCT03003117Attivo, non reclutanteAttività fisica | Crescita | Dieta | Comportamento sedentario | Infante
-
NCT02058745CompletatoTumori cerebrali maligni primari
-
NCT02816697CompletatoSmettere di fumare | Cancro ai polmoni
-
NCT03200899Completato