The feasibility of the PAM intervention to support treatment-adherence in people with hypertension in primary care: a randomised clinical controlled trial
The feasibility of the PAM intervention to support treatment-adherence in people with hypertension in primary care: a randomised clinical controlled trial
The PAM intervention is a behavioural intervention to support adherence to anti-hypertensive medications and therefore to lower blood pressure. This feasibility trial recruited 101 nonadherent patients (54% male, mean age 65.8 years) with hypertension and high blood pressure from nine general practices in the UK. The trial had 15.5% uptake and 7.9% attrition rate. Patients were randomly allocated to two groups: the intervention group (n = 61) received the PAM intervention as an adjunct to usual care; the control group (n = 40) received usual care only. At 3 months, biochemically validated medication adherence was improved by 20% (95% CI 3-36%) in the intervention than control, and systolic blood pressure was reduced by 9.16 mmHg (95% CI 5.69-12.64) in intervention than control. Improvements in medication adherence and reductions in blood pressure suggested potential intervention effectiveness. For a subsample of patients, improvements in medication adherence and reductions in full lipid profile (cholesterol 1.39 mmol/mol 95% CI 0.64-1.40) and in glycated haemoglobin (3.08 mmol/mol, 95% CI 0.42-5.73) favoured the intervention. A larger trial will obtain rigorous evidence about the potential clinical effectiveness and cost-effectiveness of the intervention.Trial registration Trial date of first registration 28/01/2019. ISRCTN74504989. https://doi.org/10.1186/ISRCTN74504989 .
Kassavou, Aikaterini
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Mirzaei, Venus
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Shpendi, Sonia
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Brimicombe, James
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Chauhan, Jagmohan
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Bhattacharya, Debi
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Naughton, Felix
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Hardeman, Wendy
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Eborall, Helen
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Van Emmenis, Miranda
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De Simoni, Anna
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Takhar, Amrit
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Gupta, Pankaj
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Patel, Prashanth
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Mascolo, Cecilia
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Prevost, Andrew Toby
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Morris, Stephen
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Griffin, Simon
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McManus, Richard J.
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Mant, Jonathan
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Sutton, Stephen
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26 April 2021
Kassavou, Aikaterini
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Mirzaei, Venus
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Shpendi, Sonia
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Brimicombe, James
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Chauhan, Jagmohan
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Bhattacharya, Debi
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Naughton, Felix
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Hardeman, Wendy
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Eborall, Helen
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Van Emmenis, Miranda
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De Simoni, Anna
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Takhar, Amrit
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Gupta, Pankaj
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Patel, Prashanth
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Mascolo, Cecilia
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Prevost, Andrew Toby
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Morris, Stephen
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Griffin, Simon
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McManus, Richard J.
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Mant, Jonathan
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Sutton, Stephen
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Kassavou, Aikaterini, Mirzaei, Venus, Shpendi, Sonia, Brimicombe, James, Chauhan, Jagmohan, Bhattacharya, Debi, Naughton, Felix, Hardeman, Wendy, Eborall, Helen, Van Emmenis, Miranda, De Simoni, Anna, Takhar, Amrit, Gupta, Pankaj, Patel, Prashanth, Mascolo, Cecilia, Prevost, Andrew Toby, Morris, Stephen, Griffin, Simon, McManus, Richard J., Mant, Jonathan and Sutton, Stephen
(2021)
The feasibility of the PAM intervention to support treatment-adherence in people with hypertension in primary care: a randomised clinical controlled trial.
Scientific Reports, 11, [8897].
(doi:10.1038/s41598-021-88170-2).
Abstract
The PAM intervention is a behavioural intervention to support adherence to anti-hypertensive medications and therefore to lower blood pressure. This feasibility trial recruited 101 nonadherent patients (54% male, mean age 65.8 years) with hypertension and high blood pressure from nine general practices in the UK. The trial had 15.5% uptake and 7.9% attrition rate. Patients were randomly allocated to two groups: the intervention group (n = 61) received the PAM intervention as an adjunct to usual care; the control group (n = 40) received usual care only. At 3 months, biochemically validated medication adherence was improved by 20% (95% CI 3-36%) in the intervention than control, and systolic blood pressure was reduced by 9.16 mmHg (95% CI 5.69-12.64) in intervention than control. Improvements in medication adherence and reductions in blood pressure suggested potential intervention effectiveness. For a subsample of patients, improvements in medication adherence and reductions in full lipid profile (cholesterol 1.39 mmol/mol 95% CI 0.64-1.40) and in glycated haemoglobin (3.08 mmol/mol, 95% CI 0.42-5.73) favoured the intervention. A larger trial will obtain rigorous evidence about the potential clinical effectiveness and cost-effectiveness of the intervention.Trial registration Trial date of first registration 28/01/2019. ISRCTN74504989. https://doi.org/10.1186/ISRCTN74504989 .
Text
s41598-021-88170-2
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Accepted/In Press date: 6 April 2021
Published date: 26 April 2021
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Local EPrints ID: 491042
URI: http://eprints.soton.ac.uk/id/eprint/491042
ISSN: 2045-2322
PURE UUID: 8b5b7013-4dee-4622-9b06-25cdbafc50b3
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Date deposited: 11 Jun 2024 16:43
Last modified: 11 Jun 2024 16:45
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Contributors
Author:
Aikaterini Kassavou
Author:
Venus Mirzaei
Author:
Sonia Shpendi
Author:
James Brimicombe
Author:
Jagmohan Chauhan
Author:
Debi Bhattacharya
Author:
Felix Naughton
Author:
Wendy Hardeman
Author:
Helen Eborall
Author:
Miranda Van Emmenis
Author:
Anna De Simoni
Author:
Amrit Takhar
Author:
Pankaj Gupta
Author:
Prashanth Patel
Author:
Cecilia Mascolo
Author:
Andrew Toby Prevost
Author:
Stephen Morris
Author:
Simon Griffin
Author:
Richard J. McManus
Author:
Jonathan Mant
Author:
Stephen Sutton
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