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Technology-based Cardiac rehabilitation Therapy improves functional capacity and quality of life in women with cardiac disease.

Technology-based Cardiac rehabilitation Therapy improves functional capacity and quality of life in …
Photo by Babak Eshaghian / Unsplash
Key Takeaway
Consider TaCT for potential improvement in functional capacity and quality of life in women with stable cardiac disease.

This randomized controlled trial was conducted in an Indian outpatient cardiology department involving women with stable cardiac disease and smartphone access. The study included n=89 participants divided into intervention and control groups. The intervention group received Technology-based Cardiac rehabilitation Therapy (TaCT), while the comparator group received standard care where cardiac rehabilitation is rare. Follow-up duration was 6 months.

Primary and secondary outcomes favored the intervention for functional capacity and quality of life. Specifically, functional capacity measured by Incremental Shuttle Walk Test showed a 95% CI = 1.0 to -0.2; P = 0.002. Duke Activity Status Index results were significant with P < 0.001, and Sit-to-Stand results showed P = 0.003. Quality of life (global and all subscales) improved with P < 0.001. Heart-health behaviours regarding exercise improved with P < 0.001, and medication adherence showed P = 0.02. Anxiety levels also decreased with P = 0.002. However, there was no significant difference in blood pressure, waist circumference, or cardiac symptoms.

Safety data indicated 3 participants in intervention group experienced morbidity and 1 suffered mortality. In contrast, 9 in controls experienced morbidity only. Key limitations include single-centre design, single-blind methodology, and two parallel arms (1:1 SNOSE). Practice relevance involves demonstrating the potential of technology-based CR tailored for women in middle-income settings. Clinicians should weigh the benefits against the safety profile and study constraints.

Study Details

Study typeRct
Sample sizen = 89
EvidenceLevel 2
Follow-up6.0 mo
PublishedApr 2026
View Original Abstract ↓
AIMS: Women are under-represented in cardiac rehabilitation (CR), especially in lower-income settings. This study tested Technology-bAsed Cardiac rehabilitation Therapy (TaCT) on functional capacity, risk factors, quality of life (QoL; MacNew), heart-health behaviours (e.g. Global Physical Activity Questionnaire), cardiac symptoms (e.g. angina), and morbidity (e.g. hospitalization and procedure) in women. METHODS AND RESULTS: Single-centre, single-blind, two parallel arms (1:1 SNOSE) randomized superiority trial, undertaken in an Indian outpatient cardiology department, where women with stable cardiac disease and smartphone access were recruited. TaCT was compared with standard care (CR rare), with assessments conducted before the intervention, and 6 months later. The 6-month comprehensive intervention was delivered via several technologies. Exercise prescriptions were based on an Incremental Shuttle Walk Test (ISWT; primary outcome). Analyses were based on intention-to-treat. Fifty women were randomized to intervention, and 50 to control (n = 89; 89.0% retained). There were few tobacco users. Results for the following outcomes favoured intervention: functional capacity [ISWT effect size = 0.3 (95% confidence interval = 1.0 to -0.2), P = 0.002; Duke Activity Status Index P < 0.001; Sit-to-Stand P = 0.003], QoL (global and all subscale P's < 0.001), and heart-health behaviours (exercise P < 0.001; medication adherence P = 0.02), and anxiety (P = 0.002). There were no significant differences in blood pressure, waist circumference, or cardiac symptoms. Three participants in the intervention group experienced morbidity and 1 suffered mortality and 9 in controls experienced morbidity only. CONCLUSION: The TaCT program significantly improved functional capacity, QoL, heart-health behaviours and anxiety in women with cardiovascular disease in a middle-income country, demonstrating the potential of technology-based CR tailored for women in these settings. REGISTRATION: CTRI/2021/07/035197 URL: https://ctri.nic.in/Clinicaltrials/rmaindet.php?trialid=51810&EncHid=79231.15408&modid=1&compid=19.
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