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NCT07811947Not yet recruiting

Inspiratory Muscle Training During Hemodialysis

Impact of Inspiratory Muscle Training on Functional Capacity, Lung Volumes, Electrical Activity and Inspiratory Muscle Strength in Hemodialysed Patients

Source: ClinicalTrials.gov · Last updated 10 Sept 2026

Brief summary (registry, in English)

This study will evaluate whether inspiratory muscle training performed during hemodialysis improves inspiratory muscle strength in adults receiving regular hemodialysis. After an initial 12-week period without study-protocolized inspiratory muscle training, participants will be randomly assigned to inspiratory muscle training plus usual care or usual care alone for 12 weeks. The primary outcome is the change in maximum inspiratory pressure from baseline to Week 12. The study will also assess lung function, walking capacity, handgrip strength, electrical activity of inspiratory muscles, dyspnea, body composition, health-related quality of life, and daily physical activity.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
53 (estimated)
First submitted
16 Aug 2026
Start date
20 Sept 2026
Primary completion date
21 Dec 2026
Lead sponsor
Tecsam - Tecnologia e Servicos Medicos
NCT number
NCT07811947

What you commit to

  • Study type: Interventional
  • Planned participants: 53
  • From 20 Sept 2026 to the primary completion date, 21 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Recent history of clinically significant cardiac arrhythmia, acute myocardial infarction, unstable angina, severe valvular disease, or uncontrolled hypertension
  • Medical condition that contraindicates an increase in intrathoracic negative pressure or performance of inspiratory muscle training
  • Uncontrolled acute or decompensated medical condition that compromises participant safety or the validity of the assessments
  • Severe cognitive impairment that prevents provision of informed consent or completion of study procedures

Who the study is looking for

  • Age 18 years or older
  • Enrolled in a regular hemodialysis program for at least 3 months
  • Receiving hemodialysis three times per week
  • Able to understand study information
  • Able to provide written informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tecsam - Tecnologia e Serviços Médicos
Coordinator of this site? Confirm its status
MirandelaPortugalUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.