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A clinical study to determine the effect of mobile phone application in improving compliance to prescribed drugs among patients with chronic diseases.

Not Applicable
Conditions
Health Condition 1: C910- Acute lymphoblastic leukemia [ALL]Health Condition 2: C921- Chronic myeloid leukemia, BCR/ABL-positiveHealth Condition 3: I10- Essential (primary) hypertensionHealth Condition 4: C50- Malignant neoplasm of breastHealth Condition 5: C34- Malignant neoplasm of bronchus andlungHealth Condition 6: C15-C26- Malignant neoplasms of digestive organsHealth Condition 7: E11- Type 2 diabetes mellitus
Registration Number
CTRI/2020/10/028420
Lead Sponsor
JIPMER Puducherry
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Diabetes mellitus and Systemic hypertension:

1. Patients with type 2 diabetes (T2DM) aged greater than 18years irrespective of gender, who are on stable dose of anti-diabetic medication for at least 1 month

2. Patients with Systemic hypertension aged greater than 18years irrespective of gender, who are on stable dose of antihypertensive medication for at least 1 month

3. Patients with concomitant type 2 diabetes and systemic hypertension

4. Patients who are able to read Tamil/ English/ Hindi

5. Patients who are owning and operating a smartphone at least for 3 months

6. Patients who are using the smartphone daily, having the phone within reach and checking it atleast three times a day

7. Patients who have not used any medication adherence application till now

Cancer:

8. Patients with gastro-intestinal malignancies receiving capecitabine

9. Patients with chronic myeloid leukemia receiving imatinib

10. Patients with breast cancer receiving hormonal therapy (tamoxifen)

11. Patients with lung cancer receiving gefitinib

12. Patients with Acute lymphoid leukemia receiving methotrexate/ 6-mercaptopurine

13. Patients who are able to read Tamil/ English/ Hindi

14. Patients who are owning and operating a smartphone for at least 3 months

15. Patients who are using the smartphone daily, having the phone within reach and checking it atleast three times a day

16. Patients who have not used any medication adherence application till now

Exclusion Criteria

Diabetes mellitus and Systemic hypertension:

1. Diabetic patients on insulin therapy

2. Patients with secondary hypertension or gestational hypertension

3. Patients with hypertensive emergency/ urgency

4. Pregnant or lactating women

5. Patients with hepatic/ renal impairment

6. Patients with h/o Coronary artery disease, cerebrovascular disease, stroke, Myocardial Infarction(MI) in the past 3 months

7. Patients who had participated in any other trials in the past 3 months

8. Patients with h/o surgery in the past 3 months or planning for surgery in the next 3 months

9. Patients on herbal medications

Cancer:

10. Pregnant or lactating women

11. Patients with h/o surgery in the past 3 months or planning for surgery in the next 3 months

12. Patients with hepatic/ renal impairment

13. Patients with h/o Coronary artery disease, cerebrovascular disease, stroke, MI in the past 3 months

14. Patients who had participated in any other trials in the past 3 months

15. Patients on herbal medications

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Adherence to medication (measured using pill count and Medication Adherence Rating Scale(MARS) /Morisky Medication Adherence Scale-8(MMAS-8)) in patients with chronic diseases (Diabetes Mellitus/ Hypertension/ Cancer)Timepoint: After 3 months
Secondary Outcome Measures
NameTimeMethod
Diabetes mellitus / Systemic hypertension: <br/ ><br>To determine the <br/ ><br>Changes in HbA1c levels in diabetes patients <br/ ><br>Changes in systolic and diastolic BP values in hypertension patients <br/ ><br>Changes in HbA1c levels, systolic and diastolic BP values in patients with concomitant diabetes and hypertension <br/ ><br>Changes in lipid profile in patients with concomitant dyslipidemia <br/ ><br>Cancer: <br/ ><br>Disease progression/ occurrence of metastasis/ recurrence of tumor in intervention and control group. <br/ ><br>Timepoint: 3 months
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