NCT06815185

Rehabilitation Counselling for Patients with Interstitial Lung Disease

Recruiting now Last updated 7 February 2025

What this trial tests

trial in Fibrosis, Pulmonary in 40 participants. Currently enrolling.

Timeline

15 December 2022

Primary endpoint
15 July 2027

15 July 2027

Quick facts

Lead sponsor	IRCCS Azienda Ospedaliero-Universitaria di Bologna
Status	Recruiting now
Study type	OBSERVATIONAL
Enrollment	40
Start date	15 December 2022
Primary completion	15 July 2027
Estimated completion	15 July 2027
Sites	1 location across Italy

Conditions studied

• Fibrosis, Pulmonary — all drugs for Fibrosis, Pulmonary →

Sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna — full company profile →

Who can join

18 and older, any sex, with Fibrosis, Pulmonary. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.