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The Role of a Clinical Pharmacist in Lifestyle Modification in Type 2 Diabetic Patients With Peripheral Neuropathy

Not Applicable
Conditions
Diabetic Peripheral Neuropathy
Interventions
Other: Diabetic patients with neuropathy
Registration Number
NCT03356041
Lead Sponsor
Hawler Medical University
Brief Summary

The aims of this study are to determine the prevalence of diabetic peripheral neuropathy among the diabetic patients, to determine the association between the clinical profiles of the diabetic patients (diabetes type, diabetes duration, HbA1c, body mass index, hypertension, total cholesterol) and the diabetic peripheral neuropathy DPN and the rational poly pharmacy used to control pain.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
200
Inclusion Criteria

Not provided

Exclusion Criteria
  1. History of alcohol consumption.

  2. Thyroid gland disorder.

  3. Any kidney disorder.

  4. Any conditions that could confound assessment of pain due to diabetic peripheral neuropathy.

  5. Have foot injury or open sore.

  6. Pregnant females or who plan to become pregnant during the study period.

  7. Any serious medical condition that might prevent completion or hinder compliance with exercise.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention GroupDiabetic patients with neuropathyThe intervention group will receive the three months' lifestyle modification program by a clinical pharmacist.
Primary Outcome Measures
NameTimeMethod
Estimating Summary of diabetes self-care activity (SDSCA)Three months

Assessing Lifestyle modification by summary of diabetes self-care activity (SDSCA) at baseline visit and after three months for both Intervention patients and usual care group Increases in the means of the items of the scale as Exercise, Blood sugar testing, Specific diet and Foot care in the intervention group.

Adherence to treatment according to Morisky scaleThree months

Morisky scale is used to assess medication adherence at baseline visit and after three months for both Intervention patients and usual care group.

Improving the patient medication adherence behavior in the intervention group patients

Douleur Neuropathique 4 (DN4), Neuropathic Pain Scale (NPS),Three months

Reduction in the percent of response of patients feeling; electric shock, tingling, and pin needle after the lifestyle modification in the intervention group.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Prof. Kawa Dizaye

🇮🇶

Erbil, Iraq

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