Dyslipidemias
Conditions
Brief summary
A randomized, parallel two-arm interventional study, the patients were divided into 1:1 ratio, in which both groups offered optimal pharmacological therapy also one group (interventional) offered predesign pharmaceutical care plan aimed to improved patients knowledge, adherence, satisfaction, and quality of life, while the other group (non-interventional) received conventional pharmaceutical care plan.
Interventions
BEHAVIORALPharmaceutical care plan
The design of the intervention was based on a stepwise approach to address the following point in each participant: set priorities for patient care, assessment of patient's educational needs, and development of a comprehensive and achievable pharmaceutical care plan. The participants will be educated about their illness and informed about the proper use of their medication in a structured manner (it involved the following items: dyslipidemia as a disease, complications, who therapy reduces its risk and complications, goal of therapy). Behavioral modifications will involve the following: physical exercise, diet, smoking cessation. Patients will obtain this information verbally and provided in a written manner through a brochure that design for this study.
Sponsors
Al-Rasheed University College
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
Patients diagnosed with dyslipidemia and received at least one statin therapy (in the previous 6 months), and patients on the same class of pharmacological therapy (statins).
Exclusion criteria
1. Pregnant women 2. Nephrotic syndrome 3. Active steroid user 4. Hypersensitivity for any mediation during the trial 5. History of a major cardiovascular event in the previous 3 months 6. Patients with mental disease or disability 7. Had a stroke in the previous 6 months
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in the quality of life in intervention group vs. non-intervention group | Baseline, and At 6 months | The RAND 36-items score (SF-36) for quality of life (QoL): This score composed of 36-items that contain 8 domains, the score has a range from 0 - 100 which represents the average of these domains. Unit of Measure is units on a Scale of 100 |
| Change in the patient satisfaction | Baseline, and At 6 months | Pharmaceutical Care Satisfaction Questionnaire (PCSQ) score for patient satisfaction: A 30-items score each item composed of a 5-point Likert scale (5 = strongly agree and 1 = strongly disagree), then the items are averaged and presented (value between 1 - 5) Unit of Measure is units on a Scale of 5 |
| Change in the medication adherence in intervention group vs. non-intervention group | Baseline, at 3 months, and at 6 months | Visual Analogue Scale (VAS) for medication adherence: The participants will be asked to mark a line at the point along a continuum showing how much of each drug they have taken in the past month, this scare take range from 0 - 10. Unit of Measure is units on a Scale of 10 |
| Change in the hyperlipidemia-Patient Knowledge in intervention group vs. non-intervention group | Baseline, and At 6 months | Hyperlipidemia-Patient Knowledge Evaluation score: The Hyperlipidemia-Patient Knowledge Evaluation is a 17-item true-or-false questionnaire, which involved general knowledge, habit, diet, pharmacotherapy, and complications. The score ranges from 0 - 16. Unit of Measure is units on a Scale of 16 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Serum LDL in intervention group vs. non-intervention group | Baseline, and At 6 months | Change in serum LDL that will occur in both the intervention group and non-intervention group, and determine which group will provide a more significant reduction in serum LDL. Unit of Measure is mg/dL |
| Change in Serum HDL in intervention group vs. non-intervention group | Baseline, and At 6 months | Change in serum HDL that will occur in both the intervention group and non-intervention group, and determine which group will provide a more significant reduction in serum HDL. Unit of Measure is mg/dL |
| Change in Serum cholesterol in intervention group vs. non-intervention group | Baseline, and At 6 months | Change in serum cholesterol that will occur in both the intervention group and non-intervention group, and determine which group will provide a more significant reduction in serum HDL. Unit of Measure is mg/dL |
| Rate of Medication-related problems manged | Up to 6 months | Each successful management of medication-related problems reported by the patients by the pharmacist will be recorded and compared between the intervention group vs. non-intervention group Unit of measure is the percentage |
Countries
Iraq
Outcome results
None listed