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NCT Number: NCT07698418

Effect of Inspiratory Muscle Training on Knee Osteoarthritis Pain

Knee osteoarthritis (KOA) is a common joint disease that causes chronic pain and limits daily activities. Current treatments, such as painkillers or surgery, have limitations like side effects or high costs. This study will test whether a safe, non-drug intervention-inspiratory muscle training (breathing exercises against resistance)-can reduce knee pain in people with KOA. The training may work by lowering inflammation and improving the brain's modulation of pain.

Eighty patients aged ≥55 years with confirmed KOA and frequent knee pain will be enrolled. Participants will be randomly assigned to either an 8-week inspiratory muscle training program (5 sessions per week, with gradually increasing resistance) or a sham (very low resistance) training program. Neither the patients nor the researchers assessing the outcomes will know who is in which group.

The main outcome is change in knee pain measured by a visual analog scale (VAS). Secondary outcomes include blood markers of inflammation (TNF-α, IL-6, IL1β), physical function, the Knee injury and Osteoarthritis Outcome Score (KOOS), inspiratory muscle strength, activity level, sleep quality, and quality of life. To explore underlying mechanisms, outcomes included heart rate variability (HRV) as an indicator of autonomic nervous system function, and brain functional connectivity in the prefrontal cortex using functional near-infrared spectroscopy (fNIRS) are collected. These mechanistic assessments will be performed at baseline and at the end of 8-week intervention. Additional follow-up assessments for clinical outcomes will be done at 3 and 6 months after the training ends. Any side effects or adverse events will be recorded.

This study will provide high-quality evidence on whether inspiratory muscle training is an effective and safe complementary treatment for knee pain in people with knee OA, and will offer new insights into the mechanisms underlying its analgesic effects.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 55 years or older.
  • Knee osteoarthritis (Kellgren-Lawrence grade ≥ 2).
  • Knee pain (Visual Analogue Scale, VAS ≥ 3) on the most days in the past month.
  • Able to walk independently without assitive devices.

Exclusion criteria

  • History of knee replacement surgery, meniscus surgery, or ligament surgery.
  • Received corticosteroid injection within the previous three weeks.
  • Diagnosed with rheumatoid arthritis.
  • Unstable angina, recent myocardial infarction, uncontrolled cardiac arrhythmia, or severe heart failure.
  • History of stroke.
  • Currently receiving steroid therapy, hormonal therapy, or cancer chemotherapy.
  • Pneumothorax, pulmonary bullae, lung surgery within the past 12 months, unstable asthma, or severe dyspnea at rest.
  • Unable to understand the study procedures and potential risks.

Treatment and study plan

Inspiratory Muscle Training

Other

Participants will perform home-based inspiratory muscle training using a threshold-loading device (POWERbreathe Medic Plus). Training is conducted 5 times per week for 8 weeks. The initial inspiratory load is set at 50% of the individual's maximum inspiratory pressure (MIP), measured weekly at the study site. The load is progressively increased to 80% MIP over the first 4 weeks and maintained at 80% MIP for the remaining 4 weeks. Each session consists of 40-60 breaths. Adherence is monitored via an electronic training log and weekly on-site visits. This protocol is individualized, progressive, and home-based, distinguishing it from fixed-load or supervised-only breathing interventions.

Other names: Respiratory muscle training

Sham inspiratory muscle training

Other

Participants will perform home-based inspiratory muscle training using a threshold-loading device (POWERbreathe Medic Plus). Training is conducted 5 times per week for 8 weeks. The initial inspiratory load is set at 10% of the individual's maximum inspiratory pressure (MIP), measured weekly at the study site. The load is maintained 10% MIP over 8 weeks. Each session consists of 40-60 breaths. Adherence is monitored via an electronic training log and weekly on-site visits.

Primary outcomes

  1. Visual analogue scale

    Time frame: Baseline, week 8, 3-month after intervention, 6-month after intervention

    Self-rated pain intensity of knee (0-100), "0" indicate no pain, "100" indicate worst pain.

Secondary outcomes

  1. The Knee injury and Osteoarthritis Outcome Score

    Time frame: Baseline, week 8, 3-month after intervention, 6-month after intervention

    Patient-reported outcomes in pain, symptoms, daily living activities, sports and recreational activities, and quality of life, with the score of each subscale ranging from 0-100, where higher scores indicate worse conditions.

  2. Serum levels of inflammatory markers

    Time frame: Baseline, up to week 8

    Systemic inflammation

  3. Heart rate variability

    Time frame: Baseline, up to week 8

    Vagus nerve activity

  4. Prefrontal cortex activity

    Time frame: Baseline, up to week 8

    Functional near-infrared spectroscopy is used to assess prefrontal cortex activity

  5. 40-meter walk test

    Time frame: Baseline, up to week 8

    Physical function

  6. 30-sec chair stand test

    Time frame: Baseline, up to week 8

    Physical function

  7. Physical Activity Scales for the Elderly

    Time frame: Baseline, week 8, 3-month after intervention, 6-month after intervention

    Total scores range from 0-793, where the higher scores indicate a higher level of physical activity.

  8. Pittsburgh Sleep Quality Index

    Time frame: Baseline, week 8, 3-month after intervention, 6-month after intervention

    Total scores range from 0-21, '0' indicating no difficulty and '21' indicating severe difficulties in all areas.

  9. 12-Item Short Form Health Survey

    Time frame: Baseline, week 8, 3-month after intervention, 6-month after intervention

    Total scores range from 0-100, where the higher scores indicate better physical and mental health function.

  10. Maximal inspiratory pressure

    Time frame: Baseline, up to week 8

    Inspiratory muscle strength

Other outcomes

  1. Adherence

    Time frame: Up to week 8

    Adherence is calculated from logbooks as completed versus prescribed sessions

  2. Adverse events

    Time frame: Up to week 8

    Adverse events are defined as any symptom or abnormal sign during training and graded by the Common Terminology Criteria for Adverse Events (CTCAE v6.0, 2025): Mild: resolved with rest, no medical intervention; Moderate: require minimal medical intervention (e.g., analgesics); Severe: requires medical attention or hospitalization (e.g., clinic visit)

Sponsors and collaborators

Lead sponsor

The Hong Kong Polytechnic University

Other

Collaborators

  • Zunyi Medical College

Registry information

Official study title

Effect of Inspiratory Muscle Training on Pain in Patients With Knee Osteoarthritis: A Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2030
Study completion
2030
First posted
Jul 13, 2026
Registry last updated
Jul 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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