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Homecare Integral Support Program for IPF Patients

Home Comprehensive Therapeutic Support Program in Patients With Pulmonary Fibrosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05173571
Acronym
PSPi-IPF
Enrollment
95
Registered
2021-12-30
Start date
2018-07-01
Completion date
2021-12-12
Last updated
2021-12-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Idiopathic Pulmonary Fibrosis

Keywords

Homecare patient support

Brief summary

Homecare patient support program especially designed for covering IPF patient needs, implemented for 12 months, for improving quality of life

Detailed description

The proposed comprehensive IPF home care programme consists of: 1) improving patient's quality of life (autonomy, activity, emotional well-being and symptoms), 2) reducing the number and severity of side effects associated with the anti-fibrotic drug, 3) reducing the number of hospitalisations attributable to the disease, and 4) providing a rapid response to any problem associated with the disease (after diagnosis or progression) that may cause distress or require early action.

Interventions

COMBINATION_PRODUCTComprehensive patient support program (educational, physiotherapy, nutritional, emotional)

Identification of patient needs and non-pharmacological holistic approach, including education, emotion and nutrition (nurse) and optimization of physical activity (respiratory physiotherapist)

Sponsors

Institut d'Investigació Biomèdica de Bellvitge
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Minimal intervention study, pre- and post- supportive care effects on quality of life

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* IPF patients with FVC \> 50% and DLCO \> 30%, in whom pharmacological treatment with nintedanib was started at least one month before the start of the programme.

Exclusion criteria

* Hospitalised patients or those who have been hospitalised in the previous month, due to any kind of respiratory exacerbation or due to any other respiratory cause. * Patients who are under home care controls (PADES) as this implies an advanced stage of the disease (forced vital capacity \[FVC\] less than 50% and the diffusion capacity of the lungs for carbon monoxide \[DLCO\] less than 30%) or, patients thathave a lack of autonomy due to comorbidities or respiratory failure * Patients diagnosed in incipient phase who have neither symptoms nor limitation in their usual activities. * Patients who have suffered any other life-threatening disease in the last 2 years, such as cancer or uncontrolled ischaemic heart disease. * Inability to understand the information given to the patient, relating to the legal aspects of the informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Qulity of life12 monthsK-BILD score (global and by domains)

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026