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Effect of Patient Education on Compliance and Cardiovascular Risk Parameters (FAILAKA)

25. mars 2014 oppdatert av: Dr. Samia Almusallam, Kuwait Institute for Medical Specialization

Effect of Patient Awareness and Education on Compliance and Cardiovascular Risk Factor Control

Patient's awareness of their risk factors for heart disease and their active involvement in their own management plan can help improve their adherence to treatment and their risk profile. The purpose of this study is to investigate the influence of patient education and awareness of heart disease risk factors on compliance to medication and lifestyle modification.

Studieoversikt

Status

Ukjent

Intervensjon / Behandling

Detaljert beskrivelse

Prospective cluster randomized interventional study with primary health care clinics as clusters.Clinics will be randomized to conventional care or to structured patient education in addition to care. Trained physicians will extract information from the patient medical record and will conduct a personal interview with the participants, after they finish with their routine visit, to fill a case report form (CRF)

CRF will include the following items:

  • Patient Demographics,
  • Socioeconomic: income, employment and education
  • Past Medical History
  • Smoking history
  • Alcohol use
  • Medications
  • Adherence: Morisky scale
  • Examination: BP, weight, height, waist
  • Investigations: LDL-C, HbA1C 2.Compliance/adherence to the medication will be measured by using the Morisky scale, which is a validated scale for measuring adherence in hypertension and diabetic patients among other disease.

Patients attending clinics that are randomized to structured patient education will receive education targeting all the risk factors they have. They will be informed about specific evidence -based target values they should achieve for each of the risk factors. Their compliance to prescribed medications will be encouraged and specific advice about improving compliance will be given. To achieve this physicians in the education clinics are going to use two items:

  1. Framingham Risk Score calculator.
  2. Know your numbers patient booklet.

Follow up visits will be scheduled at 2 months, 6 months and 12 months after the initial visit. For patients in both education and conventional clinics, compliance to medications will be assessed and the degree of risk factor control will also be determined through specific measurements that include number of cigarettes smoked, systolic and diastolic blood pressure, body mass index and waist circumference, HBA1C and LDL values.

Studietype

Intervensjonell

Registrering (Forventet)

2000

Fase

  • Ikke aktuelt

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

30 år til 70 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Patients with one or more CVD risk factors will be consecutively enrolled, smokers and obese patients should have an additional risk factors
  • The risk factors are based on Framingham Risk Score calculator and include smoking, high blood pressure, high blood cholesterol ,diabetes and being overweight or obese
  • All participants must be adults (30 -70 years of age) who give an informed consent
  • All participants should be of Kuwaity nationality, literate and fluent in either Arabic or English
  • Patients are likely to be available for a one year follow up

Exclusion Criteria:

  • Patients with mental disability or severe psychiatric disorder who are unable to provide informed consent or participate in educational activities.
  • Patients with severe visual or hearing disability that will prevent participation in the educational activity
  • Patients <30 years or >70 years of age
  • Illiterate patients
  • Non Kuwaity nationals
  • Patients who are not permanently resident in Kuwait
  • Patient who refuse to provide the informed consent

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Annen: Patient Education

Patient Education using the following two instruments:

  1. Framingham Risk Score calculator:
  2. Know your numbers patient booklet

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
cardiovascualr risk factor control
Tidsramme: 12 months
Cardiovascular risk factors control as assessed by the following parameters: HbA1C, Blood pressure, LDL-C, BMI and smoking cessation
12 months
medication compliance
Tidsramme: 12 months
Medication compliance as assessed by Morisky scale
12 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Etterforskere

  • Hovedetterforsker: Samia Almusallam, FRCGP, Kuwait Institute for Medical Specialization
  • Hovedetterforsker: Maleka M Serour, MRCGP/ INT, Kuwait Institute for Medical Specialization
  • Hovedetterforsker: Wafa A Rashed, FRCP, Ministry of Health -Mubarak Hospital- Cardiology unit

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. juni 2014

Primær fullføring (Forventet)

1. januar 2015

Studiet fullført (Forventet)

1. januar 2016

Datoer for studieregistrering

Først innsendt

24. mars 2014

Først innsendt som oppfylte QC-kriteriene

25. mars 2014

Først lagt ut (Anslag)

26. mars 2014

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

26. mars 2014

Siste oppdatering sendt inn som oppfylte QC-kriteriene

25. mars 2014

Sist bekreftet

1. mars 2014

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • WS964765

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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