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Completed

NCT Number: NCT00230984

IRAD2 : Patients With Respiratory Failure at Home

Title : Effects of home pulmonary rehabilitation in patients with chronic respiratory failure and nutritional depletion.

This is a randomized controlled, open clinical trial with two groups.

* first group, 100 patients : control group, patients followed with no add-on intervention * Second group, 100 patients : rehabilitation group with education, oral supplements, exercise and androgenic steroids.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

University Hospital Dominique Larrey, Limoges, France

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About this study

Title : Effects of home pulmonary rehabilitation in patients with chronic respiratory failure and nutritional depletion

State of the art :

The IRAD2 trial is evaluating a 3-month home intervention which includes education, oral supplements, exercise and androgenic steroids in undernourished patients with chronic respiratory failure. The main objective is to increase the six-minute walking distance by more than 50 m with an improvement in health-related quality-of-life. Secondary end-points include a reduction in exacerbation rates by 25%, a reduction in health-related costs and an increase in survival during the year following intervention.

Material and methods :

This interventional, multi-centre, prospective, two-armed parallel, controlled trial is being conducted in 200 patients. In both groups, "Control" and "Rehabilitation", 7 home visits are scheduled during the 3-month intervention for education purpose. In the "Rehabilitation" group, patients will receive 160 mg/d of oral testosterone undecanoate in men, 80 mg/d in women, oral dietary supplements (563 kcal/d) and exercises on an ergometric bicycle 3 to 5 times a week.

Expected results :

In the event of significant responses to intervention, this trial would validate a comprehensive and global home-care for undernourished patients with chronic respiratory failure combining therapeutic education, oral supplements, androgenic substitution and physical activity.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • well informed and consenting person
  • woman is old enough to procreate
  • Assisted respiratory treatment at home for 3 months : oxygenotherapy > 8 hours per day and/or assisted ventilation > 6 hours per day.
  • PaO2 without oxygenotherapy ≤ 8 kPa or 60 mmHg on ambient air at the beginning of assisted respiratory treatment.
  • Affection : chronic obstructive bronchopneumopathy, diffuse bronchial dilatation, non neuromuscular restrictive syndrome (pulmonary diffuse infiltration, parietal lesion) obstructive and restrictive syndrome.
  • malnourished person, one of following criteria :Body Mass Index ≤ 21kg/m2 or weight loss (10% of the previous weight) or non-fatty mass measured by 50 Hz impedancemetry ≤25th percentiles or ≤ 63% of ideal weight for women, ≤ 67% of ideal weight for men.

Exclusion criteria

  • Sleep apnea with daytime drowsiness (drowsiness scale of Epworth > 9/24)
  • Known pathology that reduce the vital prognosis at 6 months (AIDS, cancer...).
  • History of hormone dependent cancer ( breast cancer, prostate cancer), pathologic Prostate Specific Antigen.
  • Inability to follow a rehabilitation program

Treatment and study plan

Education

Behavioral

Oral dietary supplements (563 kcal/d), RESPIFOR

Drug

exercises on an ergometric bicycle 3 to 5 times a week

Behavioral

160 mg/d of oral testosterone undecanoate in men, 80 mg/d in women

Drug

Primary outcomes

  1. An increase of the six-minute walking distance by more than 50 m with an improvement in health-related quality-of-life.

Secondary outcomes

  1. Reduction in exacerbation rates by 25%

  2. Quality of life assessed by generic QOL.

  3. Reduction in health-related costs

  4. Increase in survival during the year following intervention.

Sponsors and collaborators

Lead sponsor

University Hospital, Grenoble

Other

Collaborators

  • Association AGIR à Dom,
  • Association ANTADIR ,
  • Ministry of Health, France
  • Nutricia France, swizerland),
  • Organon
  • Societe Francophone de Nutrition Enterale et Parenterale

Registry information

Official study title

Effects of Home Pulmonary Rehabilitation in Patients With Chronic Respiratory Failure and Nutritional Depletion.

Important dates

Study start
2003
Primary completion
2008
Study completion
2008
First posted
Oct 3, 2005
Registry last updated
Jul 8, 2009

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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