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Clinical Trials/NCT06016959
NCT06016959
Completed
Not Applicable

Specialist Dietetic Intervention in Malnourished Patients with Fibrotic ILD: a Randomised Controlled Pilot Trial

Royal Brompton & Harefield NHS Foundation Trust1 site in 1 country40 target enrollmentJune 20, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Interstitial Lung Disease
Sponsor
Royal Brompton & Harefield NHS Foundation Trust
Enrollment
40
Locations
1
Primary Endpoint
Recruitment rate
Status
Completed
Last Updated
last year

Overview

Brief Summary

Malnutrition occurs when the body receives too few nutrients, resulting in health problems such as weight loss. The consequences of malnutrition are worrying as they include lung failure, infection, and pressure ulcers.

Interstitial Lung Disease (ILD) is a term used for a group of diseases which can cause scarring of the lungs. Having ILD can cause malnutrition due to the lungs working hard and burning off energy. Additionally, medications called anti-fibrotic agents are used to slow disease progression. However, side effects include poor appetite, diarrhoea, nausea, vomiting and weight loss which can result in malnutrition.

Malnutrition occurs in ILD in approximately half of patients. This is important because the main signs of malnutrition such as weight loss and a low Body Mass Index (BMI), which takes into consideration your weight against your height, are linked with worse outcomes in ILD. Malnutrition in ILD can also reduce eligibility for lung transplant and can impact tolerability of anti-fibrotic agents. Research into treatment of malnutrition in ILD is limited.

Dietitians play a key role in diagnosis and treatment of malnutrition. This is because dietary counselling by a dietitian has been shown to increase quality of life and intake of energy in other chronic diseases. There are currently no studies documenting the benefits of dietetic intervention in patients with ILD.

We propose to undertake the first feasibility study in this area. A feasibility study is a first step trial which investigates whether a study can & should be done. The main aims of this study are:

  1. How easy it is to recruit ILD patients to see a dietitian
  2. Whether patients will attend dietetic appointments
  3. Whether food/nutrient intake is increased following dietetic intervention
  4. How acceptable is dietetic intervention to ILD patients As well as these main aims, this study will also provide initial information about whether dietetic intervention stabilises weight, BMI & quality of life.
Registry
clinicaltrials.gov
Start Date
June 20, 2023
End Date
June 1, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • BMI ≤ 20kg/m2, or if aged \>75, BMI ≤ 21 (Righini et al., 2013)
  • Over the past 12 months, unintentional weight loss ≥ 5% of body weight, regardless of baseline BMI or weight loss \>2 kg if BMI is normal.

Exclusion Criteria

  • Co-morbidities currently requiring a specialised diet (including enteral feeding)
  • End of life care (estimated less than 6 weeks left to live)
  • Expected introduction of anti-fibrotic or immunosuppressive treatment or introduction/increase corticosteroid dose during trial period
  • Pregnancy
  • Unable to give consent

Outcomes

Primary Outcomes

Recruitment rate

Time Frame: 8 months

Number individuals recruited/Number individuals contacted

Compliance

Time Frame: Defined by increased energy & protein intake versus run-in (three-day diet-diaries).

3 months

Completion rate

Time Frame: 3 months

Number individuals completing study/Number individuals randomised

Secondary Outcomes

  • Nutritional status (Malnutrition)(3 months)
  • Nutritional status (gastrointestinal related symptoms)(3 months)
  • Handgrip strength(3 months)
  • Anthropometrics (weight)(3 months)
  • Anthropometrics (height)(3 months)
  • Anthropometrics (Body Mass Index)(3 months)
  • Quality of Life (QoL)(3 months)
  • Energy and Protein intake(3 months)

Study Sites (1)

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