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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 COPD

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07803900
Acronym
COPD TEDS
Enrollment
42
Registered
2026-09-04
Start date
2025-01-28
Completion date
2025-05-30
Last updated
2026-09-04

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

Conditions

Chronic Kidney Disease, Frailty

Keywords

Renal rehabilitation, chronic Kidney disease, functional capacity, pulmonary functions

Brief summary

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 41 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.

Detailed description

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. • Aerobic Training: Aerobic exercise included cycle ergometer. Exercise intensity was maintained at approximately 40-60% of maximum heart rate and RPE 11-13. Aerobic exercise was initially performed for approximately 20-30 minutes and progressively increased by 5 minutes every 2 weeks according to tolerance, up to a maximum of 60 minutes. • Resistance Training: Exercises were performed for major upper- and lower-limb muscle groups using free weights. The initial resistance was approximately 50% of 10RM, with 10 repetitions per set. Exercises included functional lower-limb and upper-limb strengthening such as sit-to-stand, knee extension, heel raises, biceps curls and shoulder exercises. Rest intervals of approximately 1-2 minutes were provided between exercises/sets. Resistance was progressively increased according to the participant's tolerance and ability to complete the prescribed repetitions with proper technique. • Inspiratory Muscle Training: IMT was performed using a Threshold Inspiratory Muscle Trainer. Participants performed 5 sets of 10 breaths per session, with 1minute rest between sets. Training intensity was progressively increased according to MIP: 50% MIP during weeks 1-3, 60% during weeks 4-6, 70% during weeks 7-9 and 80% during weeks 10-12, as tolerated. 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 * Nephrologist: Conducted the initial CKD assessment, staging, medication review, blood pressure assessment and medical clearance before starting rehabilitation (Week 1). Medical review was repeated at Week 4, Week 8 and Week 12, or earlier if clinically indicated, to assess medical problems and exercise safety. * Renal dietitian: Provided individualized renal dietary counselling at Week 1, including appropriate protein and energy intake, sodium, potassium, phosphorus and fluid management according to CKD stage and laboratory findings. Dietary follow-up was conducted at Week 4, Week 8 and Week 12 to reinforce dietary adherence and modify recommendations when required. * Nurse: Monitored vital signs and exercise-related symptoms during every rehabilitation session throughout Weeks 1-12. The nurse also provided patient education, reinforced adherence to the exercise programme and coordinated with the rehabilitation team. Additional monitoring was performed whenever clinically required. 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.

Interventions

: 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.

BEHAVIORALInspiratory muscle training (IMT)

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.

Sponsors

Maharashtra University of Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

Group A - Experimental group received Renal rehabilitation which includes Aerobic training, Resistance training & Inspiratory muscle training along with multidisciplinary care

Eligibility

Sex/Gender
ALL
Age
40 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

\- Participants were medically diagnosed with moderate COPD (GOLD stage II-III) and were 40-70 years of age. Eligible participants included both males and females who were clinically stable, had the ability to understand and follow study instructions, and had a maximal inspiratory pressure (MIP) below 60 cmH₂O in males or below 50 cmH₂O in females

Exclusion criteria

* Patients were excluded if they had an acute COPD exacerbation, a cardiac pacemaker, unstable cardiovascular disease such as recent myocardial infarction or unstable angina, uncontrolled hypertension, or recent fractures.

Design outcomes

Primary

MeasureTime frameDescription
Diaphragm excursionBefore and after 8 weeksDiaphragm 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.
Maximal inspiratory pressurebefore and after 8 weeksMeasured by manometer
Pulmonary functionbefore and after 8 weeksMeasured by PFT device known as SP 10 BT. Components were FEV1, FVC
Six minute walk distancebefore and after 8 weeksMeasured by six minute walk test

Secondary

MeasureTime frameDescription
Modified research council scale (mMRC)before & after 8 weeksIt is a scale has 4 components with grading according to the dysnea level
COPD assessment test scoreBefore and after 8 weekshealth status related quality of life scales for COPD patients specifically.

Countries

India

Contacts

PRINCIPAL_INVESTIGATORDr.Minaz J Naik, MPT (Pursuing) (CVRS)

MAHARASHTRA INSTITUTE OF PHYSIOTHERAPY, MIMSR CAMPUS, LATUR

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 5, 2026