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NCT Number: NCT06815185

Rehabilitation Counselling for Patients with Interstitial Lung Disease

Idiopathic pulmonary fibrosis (IPF) is a rare chronic progressive disease of unknown etiology that affects physical and emotional well-being. It is characterized by irreversible loss of lung function due to fibrosis, which manifests itself with cough, dyspnea, and impaired quality of life. Lung transplantation is limited to a minority of patients and patients receive anti-fibrotic therapy in addition to supportive/palliative treatments. In light of the broad definition of pulmonary rehabilitation, and by virtue of the multidisciplinary nature of the process, the present study aims to observe the effects of the rehabilitation counseling offered to patients who attend the IPF clinic at the Pneumology Operating Unit of the IRCCS Company Bologna University Hospital, as part of the Intercompany PDTA (diagnostic therapeutic care path) for Pulmonary Fibrosis: the Intercompany PDTA for patients suffering from idiopathic pulmonary fibrosis involves a multidisciplinary approach which, also through therapeutic education/counselling, aims among others to "Offer the patient the opportunity to participate in clinical studies to increase knowledge about the disease and/or have access to innovative treatments". Primary objectives

1. Evaluate the effectiveness of the rehabilitation intervention contained in the PDTAI (Intercompany diagnostic therapeutic care path ) 2. Evaluate the improvement in functional capacity and cardiorespiratory endurance.

Secondary objectives 3. Evaluate the progress and evolution of the pathology. 4. Evaluate the emotional burden of the caregiver in caring for the individual suffering from IPF 5. Evaluate the improvement in quality of life. 6. Evaluate the change in disability. 7. Evaluate the patient's fatigue and its evolution over the course of the disease. Fatigue is associated with dyspnea, impacts daily living activities and quality of life. 8. Evaluate the progress and evolution of dyspnea at rest and in relation to the performance of common daily activities.

The study plans to enroll 40 patients newly diagnosed with IPF

Inclusion criteria:

* adulthood ≥18 years * Obtaining the patient's informed consent

Exclusion criteria:

* diagnosis of cancer in the active phase * Situations of clinical instability, of clinical worsening such as to deem the individual unsuitable for treatment because they are no longer able to go to follow up visits The included patients will receive the therapeutic education brochure from the physiotherapist and will be trained to perform the exercises during hospital visits. The physiotherapist will be able to evaluate and modify the retraining program based on the user's response according to the principles based on the individualized rehabilitation project. The direct comparison with the user allows to obtain a functional improvement adapted to the needs and performance of the person but at the same time, according to the principles of empowerment, helps the subject to become aware of their functional limits and address them with a more personalized.

The sessions will be planned following the criteria of frequency, intensity, time and type of exercise:

Frequency: one meeting/every fifteen days in the first month and one meeting every fifteen days (+/- five days) in the second and third months.

Intensity: sixty minutes (with mBorg three dyspnea and minimum peripheral saturation 88%) Time: sixty minutes Type of treatment: exercises from the therapeutic education brochure.

Endpoints measures:

1. % of patients participating in the physiotherapy session programme. It is expected that at least 80% of the total enrolled participants will participate in the proposed session cycle. 2. Six Minute Walking Test. This test is validated for multiple pathologies, including idiopathic pulmonary fibrosis. 3. % Survival of IPF patients. 4. Caregiver Strain Index. 5. EuroQoL scale. 6. Barthel Index Dyspnea. 7. Fatigue Assessment Scale. 8. Modified British Medical Research Council.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Bologna, 40138, Italy

Location status: Recruiting

Location contact

Enrica Cavalli Cavalli, MD

CONTACT

[email protected]

00390512142286

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • age>/= 18 years old;
  • Obtaining the patient's informed consent

Exclusion criteria

  • Diagnosis of active cancer
  • Situations of clinical instability, clinical aggravation such as to consider unsuitable the individual to treatment because he or she is no longer able to go to follow-up visits

Treatment and study plan

Primary outcomes

  1. Effectiveness of the rehabilitation intervention contained in the PDTAI (Inter-company diagnostic and therapeutic pathway)

    Time frame: 56 months

    % of patients participating in the physiotherapy session program, at least that 80% of the total enlisted participate in the cycle of sessions proposed.

  2. Improvement of functional capacity and cardiorespiratory endurance

    Time frame: 56 months

    Six Minute Walking Test (6MWT). This test is validated for multiple pathologies, including idiopathic pulmonary fibrosis. MCID range from 21.7 to 45 meters. One reduction of more than 50 meters in 6 months increases mortality by three times

Secondary outcomes

  1. % Survival of patients with IPF.

    Time frame: 56 months

    % Survival of patients with IPF.

  2. Caregiver Strain Index

    Time frame: 56 months

    Evaluate the emotional burden of the caregiver in assisting the affected person by IPF

  3. EuroQoL scale (EQ-5D-5L)

    Time frame: 56 months

    Evaluate the improvement in quality of life

  4. Barthel Index Dyspnea

    Time frame: 56 months

    Evaluate the modification of disability

  5. Fatigue Assessment Scale (FAS)

    Time frame: 56 months

    Evaluate the patient's fatigue and its evolution during the course of the disease. Fatigue is associated with dyspnea, impacts daily life activities and quality of life.

  6. Modified British Medical Research Council (mMRC)

    Time frame: 56 months

    Evaluate the trend and evolution of dyspnea at rest and in relation to completion of common daily activities

Study contacts

Contact information is provided by the study sponsor or research team.

Enrica Cavalli, MD

CONTACT

[email protected]

0512142285

Sponsors and collaborators

Lead sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Other

Registry information

Important dates

Study start
2022
Primary completion
2027
Study completion
2027
First posted
Feb 7, 2025
Registry last updated
Feb 7, 2025

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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