Stroke Clinical Trial
— PINGSOfficial title:
Phone-based Intervention Under Nurse Guidance After Stroke
Verified date | April 2017 |
Source | Medical University of South Carolina |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This research seeks to develop a culturally-acceptable, effective, and sustainable way of utilizing the rapidly growing penetration of mobile phones among people in Sub-Saharan Africa (SSA), to improve the currently poor control of hypertension among patients at high risk for future stroke. It also aims to develop human capital in SSA to conduct locally-relevant, high-quality stroke research in the future. Specifically, this study will preliminarily test a strategy that incorporates mobile phone texting and home blood pressure monitoring directed by trained nurses, to improve patient adherence to proven medical therapies for treating hypertension.
Status | Completed |
Enrollment | 60 |
Est. completion date | July 2017 |
Est. primary completion date | July 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Above the age of 18 years; male or female 2. Index stroke symptoms began no greater than one month before enrollment 3. Uncontrolled hypertension (SBP =140 mmHg) based upon last inpatient or outpatient encounter clinic within previous 12 months 4. Legally competent 5. Owns or has close home-sharing family member with a cell phone Exclusion Criteria: 1. Failure to meet any inclusion criteria 2. Severe cognitive impairment/dementia (Modified Mini-Mental Score [MMSE] =24)* 3. Severe global disability (modified Rankin Scale Score [mRS] = 3)* 4. Renal dialysis; awaiting renal transplant or transplant recipient 5. Cancer diagnosis or treatment in past 2 years 6. Planned pregnancy 7. Vulnerable populations such as pregnant or nursing women, prisoners, and institutionalized individuals. - MMSE =24 and global disability (mRS = 3) excludes patients who have severe cognitive impairments and medical limitations that would interfere with adequate participation in the PINGS project. |
Country | Name | City | State |
---|---|---|---|
Ghana | Kwame Nkrumah University of Science and Technology | Kumasi |
Lead Sponsor | Collaborator |
---|---|
Medical University of South Carolina | Kwame Nkrumah University of Science and Technology |
Ghana,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Recruitment rates | 9 months | ||
Primary | Patient Satisfaction Scales | 9 months | ||
Primary | Clinic based Blood Pressure | 9 months | ||
Primary | Retention rates | 9 months | ||
Secondary | Med Possession Ratio | 9 months | ||
Secondary | Morisky Med Adherence Scale | 9 months | ||
Secondary | Provider Satisfaction Scales | 9 months |
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