CTRI/2020/10/028420
Not yet recruiting
未知
Influence of smart phone application based intervention on medication adherence in patients with chronic diseases-A Randomized controlled trial.
Overview
- Phase
- 未知
- Intervention
- Not specified
- 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
- Sponsor
- JIPMER Puducherry
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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
- •8\. Patients with gastro\-intestinal malignancies receiving capecitabine
- •9\. Patients with chronic myeloid leukemia receiving imatinib
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
Outcomes
Primary Outcomes
Not specified
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