Rheumatoid Arthritis Clinical Trial
— DRAMATICOfficial title:
Impact of Pharmacist Intervention on Disease Knowledge, Rehabilitation and Medication Adherence, Treatment Induced Direct Cost, Health-related Quality of Life and Satisfaction in Patients With Rheumatoid Arthritis: a Randomized Single-blind Two-arm Controlled Trial
NCT number | NCT03827148 |
Other study ID # | USM |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | November 17, 2018 |
Est. completion date | July 1, 2019 |
Verified date | March 2020 |
Source | University of Science Malaysia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this study was to evaluate effectiveness of pharmacist intervention in
improving disease knowledge, adherence to treatment, health related quality of life and
direct cost of treatment. The study also documented patient satisfaction with pharmacist
counselling as a quality control measure.
This is a randomized controlled single-blind two-arm trial in patients with rheumatoid
arthritis in Karachi, Pakistan. The study will enroll patients with established diagnosis of
rheumatoid arthritis over three months. The patients after signing written consent would be
randomized through a computer-generated list in control group, i.e., usual care and
intervention group, i.e., pharmaceutical care with a ratio of 1:1. The study will take place
in three patient-visits over the course of three months. The patients would be intervened by
pharmacist in intervention group while those in control group will have usual care. Primary
outcomes include change in mean score at follow-up, i.e., week 12, for disease knowledge,
adherence to medications and rehabilitation/physical therapy, health related quality of life
(HRQoL). The secondary outcomes include change in the mean direct cost of treatment and
patient satisfaction from pharmacist counselling.
This is a novel study that evaluates the role of pharmacist in improving treatment outcomes
of patients with rheumatoid arthritis. The results of this trial could set the foundation for
future delivery of care for such patients in Pakistan. The results of this trial would be
published in a peer-reviewed journal.
Status | Completed |
Enrollment | 714 |
Est. completion date | July 1, 2019 |
Est. primary completion date | July 1, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Types of participants Inclusion criteria The patients who meet the following criteria would be invited to participate in our study: 1. Patients suffering from rheumatoid arthritis diagnosed with rheumatoid arthritis according to the 2010 ACR/EULAR criteria. 2. Patients diagnosed with RA based on above mentioned criteria for at least 3 months prior to invitation. 3. Patients aged above 18 years 4. Patients visiting out-patient clinics only. Before enrolling in the study, patients attended a study explanation session and provided a written consent to participate. Exclusion criteria Patients were excluded from the study if they had any of the following conditions: 1. Patients with musculoskeletal illnesses other than rheumatoid arthritis 2. Patients with a recent history of surgery or planned surgery for rheumatoid arthritis 3. Patients with more than three co-morbidities 4. Patients with any lab abnormalities, being treated for liver or kidney disease 5. Patients who have had a severe infection and have completed antibiotic course in the last week 6. Patients with advanced cardiovascular disease, severe allergies or a rare disease 7. Patients who are currently participating in other clinical trial or have participated in the last three months. 8. Pregnant patients, planning to become pregnant, breast feeding and females with other gynecological issues were not included. |
Country | Name | City | State |
---|---|---|---|
Pakistan | Clifton Central Hospital | Karachi | Sindh |
Lead Sponsor | Collaborator |
---|---|
University of Science Malaysia | Clifton Central Hospital |
Pakistan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rheumatoid arthritis disease knowledge | Patient knowledge regarding rheumatoid arthritis will be assessed after three months (week 12) from baseline (week 0). The Rheumatoid Knowledge Assessment Scale (RAKAS) will be used to measure rheumatoid arthritis disease knowledge. The RAKAS is a thirteen-item scale that contains questions related to knowledge, symptoms, treatment and risk factors. The items are multiple choice questions (MCQs) and correct answer awards a score while the wrong answers provides no score. A cumulative score is calculated which is interpreted as excellent, good, low and poor knowledge. | 3 months | |
Primary | Treatment adherence | Patient adherence to rehabilitation/physical therapy after three months (week 12) from baseline (week 0). The assessment of adherence to rehabilitation/physical therapy, will be done through Urdu version of General Rehabilitation Adherence Scale (GRAS). | 3 months | |
Primary | Medication adherence | Patient adherence to medication therapy after three months (week 12) from baseline (week 0). For the assessment of adherence to medication and pharmacotherapy, the Urdu version of General Medication Adherence Scale (GMAS) will be used. | 3 months | |
Primary | Health related quality of life (HRQoL) | It will be assessed after three months (week 12) from baseline (week 0).The EQ-5D-5L is a generic tool to measure health and provides a numeric value for health status of patient. The score is then calculated as per the criteria specified by the EuroQol. | 3 months | |
Secondary | Direct cost of treatment | The mean direct cost of rheumatoid arthritis treatment after three months (week 12) from baseline (week 0) in patients enrolled in control (CG) and intervention groups (IG). | 3 months | |
Secondary | Patient satisfaction | Patient satisfaction resulting from pharmacist-led pharmaceutical care. The proportion (%) of patients in the intervention group (IG) who were satisfied with the intervention after three months (week 12) from baseline (week 0). | 3 months |
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