Maharashtra Institute of Physiotherapy, Mimsr Campus, Latur
Latur, Maharashtra, 413531, India
NCT Number: NCT07803900
Chronic kidney disease (CKD) is a progressive condition that can be associated with reduced physical capacity, muscle weakness, fatigue, respiratory impairment and frailty. These problems may affect daily activities and quality of life. Exercise-based renal rehabilitation has been increasingly considered as an important part of the management of physical problems in CKD. However, evidence regarding multimodal rehabilitation in frail patients with CKD remains limited. Therefore, the present randomized controlled trial was conducted to evaluate the effect of a 12-week multimodal renal rehabilitation programme on pulmonary function, functional capacity and fatigue in patients with CKD who were classified as frail according to the Fried Frailty Phenotype. Frailty was defined by the presence of three or more of the five Fried criteria.
A total of 54 patients were screened, and 42 eligible participants were included and randomly allocated into two equal groups, with 21 participants in each group. Group A received the multidisciplinary renal rehabilitation, which included aerobic training, resistance training, inspiratory muscle training and multidisciplinary supportive care.
Group B received conventional physiotherapy along with standard medical care. The intervention was provided 3 times a week for 12 weeks. Pulmonary function was assessed using forced expiratory volume in one second, forced vital capacity and FEV₁/FVC ratio. Functional capacity was assessed using the 6-Minute Walk Test (6MWT) and the reported VO₂max measure. Fatigue was assessed using the Daily Fatigue Impact Scale. Assessments were performed before and after the intervention.
At baseline, there were no statistically significant differences between the two groups for pulmonary function, functional capacity or fatigue measures (p>0.05), indicating that the groups were comparable before the intervention. Following the 12-week intervention, significant improvements were observed within Group A for FEV₁, FVC, FEV₁/FVC ratio, 6MWD, VO₂max and D-FIS (p<0.001 for all outcomes). Significant within-group improvements were also observed in Group B for the measured pulmonary function, functional capacity and fatigue outcomes (p<0.001).
The between-group analysis showed statistically significant differences in favour of Group A for FEV₁, FVC, 6MWD, VO₂max and D-FIS (p<0.001). However, the between-group difference in FEV₁/FVC ratio was not statistically significant (p>0.05).
Thus, although both groups demonstrated improvement over time, the multimodal renal rehabilitation group demonstrated significantly greater improvement in most of the measured outcomes compared with conventional physiotherapy along with standard medical care.
The findings suggested that the multidisciplinary renal rehabilitation was effective in
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improving pulmonary function, functional capacity and fatigue in CKD patients with frailty over the 12-week intervention period. The improvement in fatigue was particularly evident from the significant reduction in D-FIS scores in Group A compared with Group B (between-group p<0.001). Similarly, the significant between group improvement in 6MWD and VO₂max (p<0.001) indicated better functional exercise capacity following the rehabilitation programme. The findings were consistent with previous research showing beneficial effects of exercise-based interventions on physical function and fatigue in patients with CKD. However, the study evaluated a combined rehabilitation programme, and therefore the individual contribution of aerobic training, resistance training, inspiratory muscle training and multidisciplinary support could not be determined separately. Other limitations included the relatively small sample size, and limited follow-up period.
Therefore, larger randomized controlled trials with longer follow-up are required to confirm the findings and determine whether the observed improvements are observed over time. Overall, the study concluded that a 12-week multidisciplinary renal rehabilitation may be a useful approach for improving pulmonary function, functional capacity and fatigue in CKD patients with frailty.
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Notify Me40 year–70 year
All sexes
Interventional
Not applicable
Latur, Maharashtra, 413531, India
Ethical clearance was obtained from the Institutional Ethics Committee before commencement of the study. A total of 54 CKD patients were screened, of whom 42 participants fulfilling the eligibility criteria were included in the study. Written informed consent was obtained from all participants. Baseline assessment was performed using Pulmonary Function Tests (FEV₁, FVC and FEV₁/FVC ratio), 6-Minute Walk Test (6MWD, VO₂max) and Daily Fatigue Impact Scale (D-FIS).
The 42 participants were randomly allocated into two equal groups of 21 participants each.
Group A - Renal Rehabilitation :
Participants received a structured renal rehabilitation programme consisting of aerobic training, resistance training and inspiratory muscle training for 3 days per week for 12 weeks.
Each session started with 5-10 minutes of warm-up, followed by the training programme and ended with 5-10 minutes of cool-down.
During all sessions, exercise intensity was individualized according to vitals stability, patient tolerance and clinical condition. Heart rate, blood pressure, SpO₂, fatigue and symptoms were monitored throughout the intervention.
Group B - Conventional Physiotherapy with standard medical care :
Group B received conventional physiotherapy with standard medical care, consisting of general upper- and lower-limb mobility exercises, diaphragmatic breathing exercises, stretching and active range-of-motion exercises for 30-40 minutes per session, 3 days per week for 12 weeks.
Multidisciplinary Care
At the end of 12 weeks, all participants were reassessed using the same outcome measures. Pre- and post-intervention data were recorded and statistically analyzed to determine the effect of renal rehabilitation on pulmonary functions, functional capacity and fatigue.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
: TEDS was delivered bilaterally using two channels and four surface electrodes. The frequency was fixed at 30 Hz, pulse duration at 400 µs, rise time at approximately 1 s, ON time at 1 s, and OFF time at 3 s. Current amplitude was individually adjusted according to participant tolerance and increased to achieve a visible or palpable diaphragmatic contraction. Electrode placement was standardized bilaterally at the 7th-8th intercostal spaces along the mid-axillary lines. Stimulation was synchronized manually with the inspiratory phase.The stimulation was synchronized with the inspiratory phase of breathing. The patient was instructed to start inspiration when the electrical stimulation started and to breathe out during the relaxation phase. The therapist monitored the patient's breathing and stimulation timing throughout the session to maintain synchronization.
Other names: TEDS
The IMT protocol used a Threshold IMT device. Training was initiated at 30% of MIP and progressed to 60% of MIP. Each session lasted 15-20 minutes and was performed three times per week for 8 weeks.
IMT: 5 sets × 10 breaths, with 1-minute rest between sets, 3 sessions/week for 8 weeks.
Other names: IMT
Time frame: Before and after 8 weeks
Diaphragm excursion was assessed using chest radiographs obtained at maximum inspiration and maximum expiration. The highest point of each hemidiaphragm during maximum expiration was identified, and a longitudinal line was drawn to the corresponding point during maximum inspiration. The distance between the inspiratory and expiratory positions was measured as diaphragm excursion. A radiographic ruler was used for correction of image magnification. The same measurement procedure was applied at baseline and after the intervention. Measurements were performed by a single assessor using a radiographic scale to account for image magnification.
Time frame: before and after 8 weeks
Measured by manometer
Time frame: before and after 8 weeks
Measured by PFT device known as SP 10 BT. Components were FEV1, FVC
Time frame: before and after 8 weeks
Measured by six minute walk test
Time frame: before & after 8 weeks
It is a scale has 4 components with grading according to the dysnea level
Time frame: Before and after 8 weeks
health status related quality of life scales for COPD patients specifically.
Maharashtra University of Health Sciences
Other
Effect of Synchronized Transcutaneous Electrical Diaphragm Stimulation Using Surged Faradic Current Combined With Inspiratory Muscle Training on Diaphragm Function and Clinical Outcomes in Patients With COPDEffect of Synchronized Transcutaneous Electrical Diaphragm Stimulation Using Surged Faradic Current Combined With Inspiratory Muscle Training on Diaphragm Function and Clinical Outcomes in Patients With COPDEffect of Synchronized Transcutaneous Electrical Diaphragm Stimulation Using Surged Faradic Current Combined With Inspiratory Muscle Training on Diaphragm Function and Clinical Outcomes
Acronym: COPD TEDS
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