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Effectiveness of Motivational Interview in Patients With Dyslipidemia (Dislip-EM)
This study has been completed.
Sponsor:
Hospital Universitario Reina Sofia
Collaborator:
Spanish Society of Family and Community Medicine
Information provided by (Responsible Party):
Luis A Perula, Hospital Universitario Reina Sofia
ClinicalTrials.gov Identifier:
NCT01282190
First received: January 21, 2011
Last updated: August 17, 2015
Last verified: August 2015
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Purpose
Evaluate the effectiveness of motivational interviewing to improve lipid control and cardiovascular risk in patients with dyslipidemia.
| Condition | Intervention |
|---|---|
| Patients With Dyslipidemia | Behavioral: Motivational interview |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | Effectiveness of Motivational Interview in Patients With Dyslipidemia Treated in Primary Care Consultations (Dislip-EM Study) |
Further study details as provided by Luis A Perula, Hospital Universitario Reina Sofia:
Primary Outcome Measures:
- lipid levels [ Time Frame: 12 months ]
Secondary Outcome Measures:
- cardiovascular risk [ Time Frame: 12 months ]
| Enrollment: | 207 |
| Study Start Date: | June 2010 |
| Study Completion Date: | March 2015 |
| Primary Completion Date: | March 2015 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Motivational interview |
Behavioral: Motivational interview
Motivational interview
|
Eligibility| Ages Eligible for Study: | 40 Years to 75 Years (Adult, Senior) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- People diagnosed with dyslipidemia
- To sign informed consent.
Exclusion Criteria:
- Secondary hypercholesterolemia.
- Familial hypercholesterolemia.
- Deficiency syndromes family high density lipoprotein.
- Subjects with a history of cardiac or cerebrovascular events.
- Other chronic health problems such as diabetes or severe COPD.
- Subjects with current diagnosis of cancer.
- Patients with hepatic or renal disorders .
- Subjects heavy drinkers.
- Patients with long standing sick leave (more than 6 months).
- Pregnant or breastfeeding.
Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT01282190
Please refer to this study by its ClinicalTrials.gov identifier: NCT01282190
Locations
| Spain | |
| Family Medicine Teaching Unit and Community | |
| Córdoba, Spain, 14011 | |
Sponsors and Collaborators
Hospital Universitario Reina Sofia
Spanish Society of Family and Community Medicine
More Information
Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Luis A Perula, Dr, Hospital Universitario Reina Sofia |
| ClinicalTrials.gov Identifier: | NCT01282190 History of Changes |
| Other Study ID Numbers: |
PI-0100/2008 |
| Study First Received: | January 21, 2011 |
| Last Updated: | August 17, 2015 |
Keywords provided by Luis A Perula, Hospital Universitario Reina Sofia:
|
dyslipidemia, motivational interview, prevention |
Additional relevant MeSH terms:
|
Dyslipidemias Lipid Metabolism Disorders Metabolic Diseases |
ClinicalTrials.gov processed this record on June 27, 2017