ISRCTN82013652
Active, not recruiting
未知
Randomised controlled trial of a very brief practitioner-delivered intervention plus a digital intervention to support medication adherence in people prescribed treatment for hypertension in primary care: the Programme on Adherence to Medication (PAM) trial
niversity of Cambridge0 sites578 target enrollmentDecember 9, 2019
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- niversity of Cambridge
- Enrollment
- 578
- Status
- Active, not recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Current inclusion criteria as of 01/12/2023:
- •Patients will be included if they satisfy all the following criteria:
- •1\. Has a diagnosis of hypertension (high blood pressure)
- •2\. Have been prescribed at least one antihypertensive (blood pressure lowering) medication
- •3\. Any Blood Pressure reading higher than 140/90 mmHg OR gaps in collecting repeat prescriptions
- •4\. Can understand English and is able to provide informed consent
- •5\. Has a mobile phone and is familiar with sending and receiving text messages
- •6\. The practice nurse or healthcare assistant is not aware of any other reason why the patient should be excluded
- •Previous inclusion criteria as of 22/10/2020:
- •Patients will be included if they satisfy all six criteria:
Exclusion Criteria
- •Current exclusion criteria as of 01/12/2023:
- •Patients will be excluded if:
- •1\. They have BP \> 200/100mm Hg or postural hypotension (\>20mm Hg systolic drop)
- •2\. They have a diagnosis of dementia or other cognitive difficulties that could affect study participation
- •3\. They have had a recent severe life\-threatening event or are under treatment for another long\-term health condition (e.g. cancer)
- •4\. They are taking part in another medication adherence intervention or digital intervention for behaviour change
- •5\. Their BP is not managed by their GP practice
- •Previous exclusion criteria:
- •Patients will be excluded if they:
- •1\. Have a diagnosis of dementia or other cognitive difficulties that could affect study participation
Outcomes
Primary Outcomes
Not specified
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