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Longitudinal Ultrasound Assessment of Diaphragmatic and Respiratory Muscle Function Following Respiratory Muscle Training in Frail Older Adults (IMT-1)

U

Universidad Francisco de Vitoria

Status

Not yet enrolling

Conditions

Respiratory Muscle Weakness
Geriatric Health
Frailty Syndrome
Age-Related Frailty

Treatments

Device: Sham Inspiratory Muscle Training
Device: Inspiratory Muscle Training

Study type

Interventional

Funder types

Other

Identifiers

NCT07258615
UFV-IMT1

Details and patient eligibility

About

This study aims to evaluate the effects of an 8-week inspiratory muscle training program on diaphragmatic and respiratory muscle function in frail older adults aged 80 years and above. Frailty is associated with reduced physical capacity, impaired respiratory performance, and a higher risk of disability. Inspiratory muscle training is a simple, low-cost intervention that may improve breathing function, strength, and overall health in very old adults, but evidence in this age group remains limited.

Participants will be randomly assigned to one of two groups: a high-load inspiratory muscle training group or a low-load sham training group. Both groups will use a threshold device and perform 30 breaths once per day, five days per week, for eight weeks. The experimental group will train with progressively increasing resistance (50% to 80% of maximal inspiratory pressure), while the sham group will use a minimal and non-progressive load (15% of maximal inspiratory pressure). All sessions will be supervised and monitored for safety.

The main goal of the study is to determine whether inspiratory muscle training improves maximal inspiratory pressure (MIP), an established measure of global inspiratory muscle strength. Secondary outcomes include ultrasound-based assessments of diaphragmatic structure and function, such as diaphragm thickness, contractile fraction, diaphragmatic excursion, inspiratory time, and inspiratory velocity during deep breathing and sniff maneuvers. These measurements will help clarify the physiological adaptations produced by inspiratory muscle training in this population.

Assessments will be performed before the intervention, immediately after the 8-week program, and again at one and three months after the end of the intervention to examine both immediate and short-term effects. This study may contribute valuable evidence regarding the safety, feasibility, and clinical benefits of inspiratory muscle training in frail very old adults, supporting its potential implementation in rehabilitation and geriatric care.

Enrollment

30 estimated patients

Sex

All

Ages

80+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults aged 80 years or older.
  • Clinical diagnosis of frailty, defined by a Short Physical Performance Battery (SPPB) score < 9.
  • Ability to stand and walk with or without assistive devices.
  • Ability to understand and follow instructions for inspiratory muscle training.
  • Stable medical condition for at least 3 months prior to enrollment.
  • Capacity to provide informed consent or availability of a legal representative.

Exclusion criteria

  • Acute or unstable cardiovascular, respiratory, or metabolic conditions.
  • Severe cognitive impairment that prevents understanding the procedures.
  • Diagnosis of neuromuscular diseases affecting respiratory muscles (e.g., ALS, myopathies).
  • Severe or uncontrolled hypertension (≥180/110 mmHg).
  • Recent thoracic or abdominal surgery (<3 months).
  • Severe musculoskeletal disorders limiting participation in training.
  • History of recurrent syncope, severe dizziness, or intolerance to respiratory maneuvers.
  • Any condition judged by the research team to compromise safety or participation.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

Inspiratory Muscle Training
Experimental group
Description:
Participants perform an 8-week inspiratory muscle training program using a threshold device (PowerBreathe). Training consists of 30 inspirations, once daily, 5 days per week. The initial load is set at 50% of each participant's maximal inspiratory pressure (MIP) and is increased weekly by 5 cmH₂O up to 80% of MIP. All sessions are supervised by healthcare professionals, with continuous monitoring of oxygen saturation and heart rate.
Treatment:
Device: Inspiratory Muscle Training
Inspiratory Muscle Training (Sham)
Sham Comparator group
Description:
Participants follow the same 8-week training schedule using the threshold device (PowerBreathe), but with a constant load of 15% of maximal inspiratory pressure (MIP) and no weekly progression. Training consists of 30 inspirations, once daily, 5 days per week. The procedure mimics the experimental intervention but provides minimal physiological stimulus. All sessions are supervised, with monitoring of oxygen saturation and heart rate.
Treatment:
Device: Sham Inspiratory Muscle Training

Trial contacts and locations

0

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Central trial contact

Jorge Sánchez-Infante, PhD, PT

Data sourced from clinicaltrials.gov

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