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CompletedNCT06029842Updated Nov 21, 2024

The Role of a Clinical Pharmacist in the Management of Type 2 Diabetic Patients in a Primary Medical Center in Jordan

An interventional study of Collaborative approach of clinical pharmacist with physicians in a medical center in Pharmacist-Patient Relations, sponsored by University of Jordan. Completed at 1 site in Jordan. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-11-21.

Sponsored by University of Jordan · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 10 months after the study started (first participant enrolled Oct 2022, registered Sep 2023).
Phase
Not applicable
Study type
Interventional
Enrollment
103
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This study aimed to assess the impact of the clinical pharmacist on enhancing type 2 diabetic patients outcomes in a primary health care center.

Read the detailed description

About 103 patients with type 2 diabetes were randomized to control or intervention group, the control group received a standard care, while the intervention group received the collaborative care between the clinical pharmacist and physicians. Fasting blood glucose, HbA1c, Lipid profile, and blood pressure measured for both groups at baseline and after three months of follow-up. Treatment related problems (TRPs), quality of life, adherence, and patients knowledge about their medications were assessed. Cost avoidance and clinical significance of implemented clinical pharmacist interventions were assessed too.

02

Conditions studied

  • Pharmacist-Patient Relations

Keywords

  • clinical pharmacist
  • medical center
  • Ministry of Health
  • Collaborative approach
03

In context

Lead sponsor

University of Jordan is the lead sponsor of 126 studies on the registry; 20 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • type 2 diabetic patients who aged 18 years or more with a HbA1c reading 6.5 % or more at the time of diagnosis

Exclusion criteria

Exclusion Criteria:

  • pregnant patients
  • breastfeeding patients
  • patients with urgent or emergent cases
  • patients with cognitive impairment
  • if the patient is unable to provide informed written consent
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
103 participants (actual)

Study arms

  • Other
    the intervention group

    this group received the collaborative care between the clinical pharmacist and physicians in a medical center

    Other: Collaborative approach of clinical pharmacist with physicians in a medical center

  • No intervention
    the control group

    this group received the standard care of physicians in a medical center without clinical pharmacist interventions

Interventions

  • OtherCollaborative approach of clinical pharmacist with physicians in a medical center

    For those who allocated to the intervention group, the clinical pharmacist interviewed them at each monthly visit about 30 minutes before seeing physicians, the clinical pharmacist identified treatment related problems, provided medication counseling, answered questions asked by patients or physicians, encouraged compliance, offered instructions on self-monitoring of blood pressure and glucose levels, distributed educational materials about diabetes and emphasis was made on optimizing adherence to pharmacological and non- pharmacological therapy. the pharmacist interventions on treatment related problems (TRPs) and proposed patient care plans were discussed with treatng physicians who decided to accept or reject them.

06

What researchers measure

Primary outcomes

  1. HbA1c

    Time frame: 3 months

Secondary outcomes

  1. Lipid profile

    LDL , HDL , TGS

    Time frame: 3 months

  2. Fasting blood glucose

    Time frame: each month for 3 months

  3. Patients knowledge about their medications

    Validated questionnaire were used. According to Abu Farha et.al, Patients' medication knowledge was assessed by their ability to answer correctly the questions related to their medication doses, indications and timing. For each correct statement the patient gained 1 point with a total of 3 points for each medication. Patients were considered to have suboptimal knowledge if they obtain an average medication score of 2 or less.

    Time frame: 3 months

  4. Cost avoidance of implemented clinical pharmacist interventions

    The cost avoidance of implemented interventions were evaluated relevant to "presumed cost avoidance". This implies an action that reduces or eliminates additional spending that would have happened if the intervention had not occurred. The reduction in costs was estimated using the cost avoidance values that were derived from Campbell. The resulting cost avoidance values for individual clinical pharmacy intervention types are listed below for individual clinical pharmacy intervention type.\* Intervention type, Overall cost avoidance, $ Addition of a medication 62.81 * Change medication 74.67 * Discontinuation of a medication 57.25 * Dosage form change 67.33 * Dose adjustment 71.41 * Drug information 26.97 * Medication reconciliation 472.86 * Monitoring laboratory order 93.58 * Non-formulary consultation 56 * Non-formulary to formulary conversion 44 * Pharmacokinetic monitoring-level adjustment 91.08 * Prevention of adverse drug event 581.08 * Prompted medical follow-up 70.33

    Time frame: 3 months

  5. Patients adherence to medications

    Patients' adherence to medications was assessed by Oriana Awwad et al.2022 validated Arabic version of the Morisky, Green, and Levine (MGL) adherence scale \[16\], This scale is "a 4-item instrument used to identify patients with chronic disease who are not taking their medications as prescribed". The scale encloses four questions: 1) "Do you ever forget to take your medicine?" 2) "Are you careless at times about taking your medicine?" 3) "When you feel better do you sometimes stop taking your medicine?" and 4) "Sometimes if you feel worse when you take the medicine, do you stop taking it?" It has a scoring scheme of "Yes" = 1 and "No" = 0 for each item with a total score ranging from 0 to 4. The sum of "Yes" answers provides a composite measure of non-adherence. Lower evaluations imply a higher level of adherence, and total patient scores can be classified into high adherence level (0 answered "yes"), moderate adherence level (1-2 answered "yes") and low level adherence (3-4 "yes").

    Time frame: 3 months

  6. Quality of life

    The change in the Quality of Life questionnaire (EQ-5D-5L) was assessed. At baseline, all patients were asked to self-complete the Quality of Life (EQ-5D-5L) questionnaire. This self-completed questionnaire consists of 5 domains" (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression)" in which each dimension is rated with 5 levels of severity (no problems, slight problems, moderate problems, severe problems, and unable to perform or extreme problems). The answers on these domains are translated to give a consequent number; e.g 23445. These numbers have a health utility index score which already had been studied and validated for different population in a number of countries. A single index value for all health states with a range from 0 (where zero is a health state equivalent to death). Another factor express QoL is EQ-vas which is a scale from 0 to 100 where the patients are asked to indicate their overall health on the day after completion of questionnair.

    Time frame: 3 months

  7. Blood pressure

    Time frame: 3 months

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Study locations

1 site
  • Abu-Nsair medical center
    Amman, Jordan
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References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 21, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06029842
Lead sponsor
University of Jordan
Responsible party
Jyana Alelaimat (Master student at the University of Jordan, University of Jordan) — Principal investigator
First posted
Sep 8, 2023
Start date
Oct 17, 2022
Primary completion
Apr 24, 2023
Completion
Apr 24, 2023
Last update
Nov 21, 2024

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2024. You cannot join it, but the record below documents what was studied.

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