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The Impact of Structured Patient Education Material (SPEM) in Improving Clinical and Behavioural Outcomes in Home-based Cardiac Rehabilitation Program Participants: A Pilot Study

The Impact of Structured Patient Education Material (SPEM) in Improving Clinical and Behavioural Outcomes in Home-based Cardiac Rehabilitation Program Participants: A Pilot Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05045118
Enrollment
20
Registered
2021-09-16
Start date
2021-03-30
Completion date
2022-06-30
Last updated
2021-09-16

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

Conditions

Ischaemic Heart Disease

Brief summary

This study aims to examine the impact of providing a digital education material to participants of home based cardiac rehabilitation in improving clinical and behavioural outcomes

Detailed description

This is a pilot study aiming to assess the impact of providing a structured patient education material in a digital form to participants of home based cardiac rehabilitation program in University Malaya Medical Centre.

Interventions

OTHERDigital Structured Patient Education Material

Participants of home-based Cardiac Rehabilitation Program that are included in this research will be provided with a digital Structured Patient Education Material at the beginning of the program, and will be followed up for 12 weeks duration

Sponsors

University of Malaya
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 20-70 years * Fulfills the low to moderate exercise participation risk criteria for Cardiac rehabilitation program phase 2 as per the American Association of Cardiovascular and Pulmonary Rehabilitation standards * Able to participate in a treadmill exercise program * Cognitively able to give consent, and able to read and utilize the digital education material

Exclusion criteria

* Stratified as high risk to participate in an aerobic exercise program as per the American Association of cardiovascular and Pulmonary Rehabilitation standards

Design outcomes

Primary

MeasureTime frameDescription
Retention rate3 monthsThe proportion of patients who completed the education material. The number of participants completed divided by the total number of participants, expressed in percentage
Cardiorespiratory fitness3 monthsPeak METs and HRmax measured by exercise stress testing, to estimate VO2 max. This measurement is recorded at pre and post 12 weeks of intervention

Secondary

MeasureTime frameDescription
Smoking status3 monthsSmoking status will be recorded as reported by patient upon recruitment, and at 1st, 2nd and 3rd month of program
Compliance to medication3 monthsCompliance to daily medication will be recorded as reported by patient upon recruitment, and at 1st, 2nd and 3rd month of program
Compliance to exercise3 monthsNumber of hours of performing aerobic exercise per week upon recruitment, at 1st, 2nd, 3rd month

Countries

Malaysia

Outcome results

None listed

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