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The Effectiveness of Multimodal Educational Intervention to Improve Adherence to Treatment Regimens in Older Stroke Patients

The Effectiveness of Multimodal Educational Intervention to Improve Adherence to Treatment Regimens in Older Stroke Patients: A Randomised Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02842840
Enrollment
405
Registered
2016-07-25
Start date
2016-04-30
Completion date
2017-11-30
Last updated
2016-07-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Medication Adherence, Older Adults, Stroke

Brief summary

Stroke is a major cause of morbidity and mortality, especially in low and middle income countries including Iran. Patients with recent stroke or TIA are at high risk for new vascular events. Several evidence based strategies in secondary prevention of stroke are available but frequently underused. The study is aimed to evaluate an intervention to improve patients with Stroke.

Interventions

BEHAVIORALPatient-based intervention

Sponsors

Qazvin University Of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* aged 65 years or older * able to give informed consent

Exclusion criteria

* recurrent stroke * a diagnosis of subarachnoid haemorrhage * significant impairments precluding participation - inability to give informed consent * another condition likely to impact their participation in the trial (e.g. life-threatening condition other than cardiovascular disease) * expected discharge to hospital/nursing home setting

Design outcomes

Primary

MeasureTime frameDescription
changes in Patient-reported Adherence Medication Adherence Rating Scalechanges from baseline, 6 Months, 12 months and 18 months follow-upa self-report measure of adherence (Medication Adherence Report Scale \[MARS-5\]) will be used .
changes in blood pressurechanges from baseline, 6 Months, 12 months and 18 months follow-up
changes in low-density lipoprotein (LDL)-cholesterol levelchanges from baseline, 6 Months, 12 months and 18 months follow-up

Secondary

MeasureTime frameDescription
Changes in quality of lifechanges from baseline, 6 Months, 12 months and 18 months follow-upThe Short Form (36) Health Survey is used to assess patient's quality of life
Changes in perceived behavioral control to medication adherencechanges from baseline, 6 Months, 12 months and 18 months follow-upThe perceived behavioral control to medication adherence is assessed through a self-report instrument
Changes in intention to medication adherencechanges from baseline, 6 Months, 12 months and 18 months follow-up
Changes in Illness Perceptionschanges from baseline, 6 Months, 12 months and 18 months follow-upthe Brief Illness Perception. Questionnaire (Brief IPQ) is used to assess patient's illness representation
Changes in Self-monitoring to medication adherencechanges from baseline, 6 Months, 12 months and 18 months follow-upThe Self-monitoring to medication adherence is assessed through a self-report instrument
Changes in Action Planchanges from baseline, 6 Months, 12 months and 18 months follow-upThe action plan is assessed by a self-reported questionnaire. it is used by the patients before, at baseline, six months, twelve months and eighteen months after the intervention
Changes in Coping Planchanges from baseline, 6 Months, 12 months and 18 months follow-upThe coping plan is assessed by a self-reported questionnaire. It is used by the patients before, at baseline, six months, twelve months and eighteen months after the intervention

Countries

Iran

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026