Introduction
One of the systems affected by aging is the cardiopulmonary system. Aging reduces cardiovascular health, and many cardiac diseases eventually lead to chronic heart failure (CHF). CHF is a condition characterized by impaired cardiac structure and function, wherein the heart cannot pump sufficient blood to meet the body’s needs, resulting in reduced oxygen and nutrient delivery. CHF is one of the most critical conditions in older adults, with its prevalence and incidence increasing with age. Respiratory exercises, including those as adjunctive treatments, have received less attention in this population. Among the latest models of respiratory training for these patients is device-guided slow breathing exercise. Accordingly, this study investigates the effect of routine respiratory exercises and device-guided gradual slow breathing exercises on the quality of life, physical performance, and blood pressure in elderly patients with CHF.
Methods
This single-blind randomized clinical trial was conducted in 2021–2022 in Mashhad City, Iran. A total of 36 patients with CHF were randomly assigned to the following three groups of 12 using a sealed-envelope method: a control group (mean age: 64.58±3.46 years), a routine breathing exercise group (mean age: 63.67±3.91 years), and a device-guided gradual slow breathing exercise group (mean age: 62.58±2.57 years). The inclusion criteria were having class II and III heart failure based on New York Heart Association (NYHA) classification, aged 60–70 years, heart failure diagnosis for 3–5 years, ejection fraction < 50%, receiving standard medication for at least one month prior to the study, no history of unstable angina or complex ventricular arrhythmias, no myocardial infarction in the past year, no cardiac pacemaker, no bypass surgery or angioplasty in the past six months, no participation in other exercise programs in the past six months, and no history of pulmonary disease, smoking, angina, heart surgery (within the past six months), orthopedic or neurological conditions, or treatment with steroids or chemotherapy. Exclusion criteria included unwillingness to continue, participation in other exercise programs, or disruption of treatment during the study.
The intervention lasted four weeks, with pre- and post-intervention assessments completed. Due to the COVID-19 pandemic, all interventions were conducted at participants’ homes following strict protocols, under the direct supervision of the researcher. Quality of life was measured using the Minnesota living with heart failure questionnaire, physical performance was assessed via the 6-min walk test, and blood pressure was measured using a blood pressure Holter monitor. The data were analyzed using the SPSS software, version 23, employing paired t-tests and one-way analysis of variance.
Results
No statistically significant differences were observed in demographic variables between the groups pre-intervention (P>0.05). Similarly, no significant changes in hemodynamic variables were noted post-intervention (P>0.05). None of the participants experienced any adverse events during the study. Comparisons of hemodynamic status within each group showed a significant improvement in peripheral oxygen saturation (SPO2) before the 6-min walk test in the gradual slow breathing exercise group (P=0.047). However, no statistically significant differences in SPO2 were observed between the three groups post-intervention (P>0.05).
Mean quality-of-life scores significantly decreased in the routine breathing group (P=0.02) and the gradual slow breathing group (P=0.007). Physical performance scores significantly increased in the routine breathing group (P=0.028) and the gradual slow breathing group (P=0.033). The one-way analysis of variance test showed a statistically significant decrease in quality-of-life scores in the routine breathing group (P=0.026) and a significant increase in physical performance scores in the gradual slow breathing group (P=0.042) compared to the control group.
In NYHA class II patients, both routine breathing exercises (P=0.02) and gradual slow breathing exercises (P=0.007) significantly improved quality-of-life scores. Physical performance scores increased significantly in the gradual slow breathing group (P=0.02) within class II patients. No significant changes were observed in class III patients or other parameters within class II (P>0.05). The one-way analysis of variance on changes in mean scores across the three groups based on NYHA classification showed statistically significant differences only in quality-of-life (P=0.01) and physical performance (P=0.02). Post hoc Bonferroni analysis revealed a significant reduction in quality-of-life scores in the routine breathing group (P=0.015) and a significant increase in physical performance scores in the gradual slow breathing group (P=0.018) compared to the control group in NYHA class II.
Conclusion
No significant changes in blood pressure were observed post-intervention, aligning with Drozdz et al’s [
52] findings in 2016 but contrasting with Lachowska et al.’s 2019 study [
23]. The discrepancy may be attributed to the differing durations of interventions in the latter study. Respiratory exercises improved quality of life, consistent with findings by Lachowska et al. (2019) [
23] and Azambuja et al. (2020) [
60] but contrasting with Drozdz et al. (2016) [
52]. These differences might stem from the very low fixed breathing rate of 6 breaths/min or differences in participants’ age range.
The exercises also enhanced physical performance and increased the six-minute walking distance, consistent with Lachowska et al. (2019) [
23], Kawecka-Jaszcz et al. (2017) [
65], and Azambuja et al. (2020) [
60]. This improvement highlights the positive impact of these exercises on the functional capacity of patients who often face daily challenges.
Ethical Considerations
Compliance with ethical guidelines
Ethical approval was obtained from the Medical Ethics Committee of Tarbiat Modares University, Tehran, Iran (Code: IR.MODARES.REC.1400.200), and the study was registered in the Iranian Registry of Clinical Trials (IRCT) (Code: IRCT20210426051093N1). After the study, the control group received a 10-session routine respiratory training program over four weeks alongside relevant medical recommendations.
Funding
This project was financially supported by Tarbiat Modares University, Tehran, Iran (Grand No.: 88223).
Authors' contributions
Conceptualization, methodology, review and editing: Roya Ravanbod and Mehdi Rahmati Yami; Supervision and investigation: All authors; Writing the initial draft: Mehdi Rahmati Yami.
Conflicts of interest
The authors declared no conflict of interest.
Acknowledgements
The researchers express gratitude to Tarbiat Modares University for financial support, as well as all participants and the following individuals: Physiotherapists Elham Azarmi and Afrooz Etedali, Mehdi Alizadeh Birjandi, Mohammad Sookhtanlou, Saeed Akhlaghi, Farhad Azadi, Majid Shahbazi, Nima Davari, and Hemmat Jamshidi.
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