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Testing breathing-related approaches in Parkinson’s

This pilot trial studies approaches involving brief increases in carbon dioxide, looking at functions such as breathing, voice and cough.

Testing a treatment or activity · Study reference: NCT07674264

Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓

Open the official registry record ↗

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Looking for volunteers

Start (reported actual date)
2026-08-12
Main measurements finished (planned)
2028-12-31
Study finished (planned)
2028-12-31

Planned dates can move. A study finishing does not tell us when a paper will be published.

No results summary has been confirmed in the registry records we imported. See connected papers below; we keep checking after recruitment ends.

Changes we have recorded
  • 2026-10-11 — recruiting

These are dates we observed a change, not necessarily the dates it happened.

Papers connected to this study

No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.

Who can join?

Ages 40 years to 75 years · Does not accept healthy volunteers

These are starting points, not the full rules. The research team can tell you whether the study is right for your situation.

Read all the rules for taking part

Sex eligibility reported by registry: all

Inclusion Criteria: 1. adults 40 to 75 years of age (the latter to reduce the likelihood of cardiovascular disease) 2. diagnosis of idiopathic Parkinsonism with Hoehn and Yahr stages 2-4 3. medically stable with physician clearance 4. ability to ambulate at least 10 feet with/without assistance 5. ability to follow directions 6. willing to abstain from blood donation for the duration of the study Exclusion Criteria: 1. additional neurologic conditions 2. severe illness or infection, including respiratory/cardiovascular/lung disease, or uncontrolled hypertension 3. inspiratory stridor 4. pregnancy due to unknown tAIH effects on a fetus, although females of childbearing age will not be excluded\* 5. cigarette smoking or vaping within 5 years 6. history of head/neck/lung cancer with the exception of basal cell carcinoma 7. is currently participating in another research study that could influence the results from this study 8. has deep brain stimulation electrodes implanted or has a history of deep brain stimulation 9. faints or becomes lightheaded at the sight of blood * If a female of childbearing potential indicates there is a chance she could be pregnant, she will be provided a pregnancy test and allowed to continue in the study if negative. This is because the fetal risks associated with intermittent hypoxia are unknown.
Full study name & original research details

Official study title

A Pilot Study of Acute Intermittent Hypercapnia-Based Interventions on Upper Airway and Axial Motor Function in Parkinson's Disease

Short title used by the registry

Cross-System Effects of Acute Intermittent Hypercapnia-Based Interventions in PD

Original description

Parkinsonism impairs upper airway and axial motor control, leading to disordered breathing, reduced speech volume, and ineffective cough. Symptoms are poorly addressed by current therapies. This randomized pilot trial tests whether a single session of acute intermittent hypercapnic hypoxia (AIHH) or hypercapnic normoxia (AIHN) improves upper airway and axial motor function in Parkinsonism, and explores biomarker correlates of intervention responsiveness.

Conditions reported: Parkinson Disease; Parkinsonism

Registry records for this study

Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.

Study type
Interventional
Interventions
Acute intermittent hypercapnic hypoxia (AIHH); Acute intermittent hypercapnic normoxia (AIHN)
Phases
NA
Sponsor
University of Florida
Start date reported by registry
2026-08-12 (actual)

Registry updated: 2026-08-21 · Status last verified by the registry submitter: 2026-06

Registry records retrieved 2026-10-11 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.

Contact the research team

Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.

Michlela Mir, CCC-SLP, PhD · 352-273-6095 · michela.mir@ufl.edu

Alysha Bogard, PhD · 3038279875 · abogard@ufl.edu

Study locations

Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.

University of Florida

Gainesville, Florida, United States

Recruiting

Michela Mir, CCC-SLP, PhD · 352-273-6095 · michela.mir@ufl.edu

Alysha Bogard, PhD · 3038279875 · abogard@ufl.edu

Michela Mir, CCC-SLP

Alysha Bogard, PhD

Norman Fixel Institute for Neurological Diseases

Gainesville, Florida, United States

Recruiting

Michela Mir, CCC-SLP, PhD · 303-827-9875 · michela.mir@ufl.edu

Alysha Bogard, PhD · 3038279875 · abogard@ufl.edu

Michela Mir, CCC-SLP

Alysha Bogard, PhD

Facility not reported

United States

Status not reported

The original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.