Nutritional Status and Intake in Patients With Non-cystic Fibrosis Bronchiectasis (NCFB)

NCT06877091 | Completed

• 1 other identifier: Version 1
• Study Type: observational
• Target: 129
• Locations: 1 country
• Sites: 1

Brief Summary

The aim of this study was to characterise nutritional status and dietary intake in a population of individuals living with bronchiectasis from a regional clinic. Participants underwent usual assessment as per their standard pathway of care and in addition, body composition through skinfold measures, Handgrip strength and information on dietary intake over 3 days via 24 hour multiple pass recalls was also collected. This was to establish baseline measures and knowledge in support of understanding the impact of nutritional status within this group.

Conditions

Non Cystic Fibrosis Bronchiectasis

Keywords

Nutritional status; Dietary Intake; NCFB

Outcome Measures

Primary Outcomes (5)

• Lung Function (FEV1 )

  Collect spirometry data that is measured as part of clinical care

  At point of recruitment

• Lung Function ( FVC)

  Collect spirometry data that is measured as part of clinical care

  At point of recruitment

• Height (m)

  Height will be taken to enable measurement of BMI

  At point of recruitment

• Weight (kg)

  Weight will be taken to provide unit to calculate BMI (kg/m2)

  At point of recruitment

• BMI (kg/m2)

  Collection of standard data (weight and height) from usual care pathway

  At point of recruitment

Secondary Outcomes (3)

• Handgrip Dynamometry (kg/f)

  At point of recruitment

• Tricep Skinfold measurement (mm)

  At point of recruitment

• Dietary intake checklist

  At point of recruitment

Study Arms (1)

Regional cohort of individuals living with Non-Cystic Fibrosis Bronchiectasis

Eligibility Criteria

• Age: 17 Years - 99 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Those who attend the Leeds Regional Bronchiectasis Clinic

You may qualify if:

• People who have a confirmed diagnosis of NCFB
• people with NCFB who are clinically stable (not requiring acute admission to hospital)
• people who attend the regional clinic

You may not qualify if:

• People who are pregnant
• people with existing comorbidities such as malignancy

Sponsors & Collaborators

• University of Leeds: lead
• The Leeds Teaching Hospitals NHS Trust: collaborator

Study Sites (1)

Leeds Teaching Hospitals Trust

Leeds, West Yorkshire, LS9 &TF, United Kingdom

Location

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: March 6, 2025
• First Posted: March 14, 2025
• Study Start: July 1, 2017
• Primary Completion: July 31, 2018
• Study Completion: July 31, 2018
• Last Updated: March 14, 2025

Record last verified: 2025-03

Locations

GB (1)