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Evaluation of a Behavioural Intervention Using App Technology in CF

Evaluation of a Behavioural Intervention Using App Technology in Cystic Fibrosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03782909
Acronym
EAT-CF
Enrollment
5
Registered
2018-12-20
Start date
2019-05-08
Completion date
2020-03-01
Last updated
2021-02-12

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

Conditions

Cystic Fibrosis

Keywords

Nutrition, Weight, BMI, Behaviour change

Brief summary

Cystic Fibrosis (CF) is a lifelong condition which causes the lungs and digestive system to become clogged with thick, sticky mucus. This leads to recurrent chest infections and reduced nutrient absorption from food. The average age at death is 31 years, usually from respiratory failure. The nutritional status of people with CF (PWCF) is important to help them live healthier and longer. It is recommended that adults with CF achieve a BMI of 23 for males and 22 for females. However, fewer than 50% of adults with CF achieved that target BMI despite effective nutritional support to help weight gain. There is a clear need for a behavioural intervention that can help PWCF use the available nutritional support. This is a feasibility study to try out a multi-component behavioural intervention supported by a nutrition app. The intervention is designed to help PWCF use their nutritional support to gain weight. It will focus on testing the methods and procedures to be used on a larger scale, improving the behavioural intervention and estimating how many people are needed for the larger trial. Eligible patients will be invited to participate, and the investigators anticipate recruiting 6 participants. The participants will have 6 weeks of intensive intervention, which will include a mix of clinic visits, home visits and telephone calls followed by 6 weeks of maintenance phase. Data will be collected during clinic visits at baseline, week 6 and week 12 along with weight monitoring at home. The investigators will interview each participant at the end of the study period to improve the intervention and study processes based on participant feedback. The investigators hypothesised that using a nutrition app, along with regular input from a dietitian, will help PWCF to use the available nutritional support.

Interventions

The behaviour change intervention consists of; 1. Feedback via an app based food diary 2. Coaching with problem solving and implementation plans The intensive phase consists of 2 home visits and 4 phone calls and the use of the app The maintenance phase consists of use of the app if the PWCF wishes to continue using it

Sponsors

Sheffield Teaching Hospitals NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

* adult people with CF looked after at the Sheffield Adult CF Centre * best BMI of \<23 for males and \<22 for females between June 2018 and November 2018

Exclusion criteria

* patients in palliative phase of disease * patients who are pregnant * patients who have no capacity to consent to participate in the study * patients who are unable to communicate by telephone for coaching

Design outcomes

Primary

MeasureTime frame
Proportion of patients who accepted invitation to participate as a marker of feasibility4 weeks

Secondary

MeasureTime frameDescription
Participant attrition rate and phases of the study whereby the attrition occurs3 months
Participants' opinion about the study processes3 monthsA semi-structured interview will be used for thematic analysis
Participants' suggestions for further improvement of the intervention and study processes3 monthsA semi-structured interview will be used for thematic analysis
Participants' opinion about the behavioural intervention3 monthsA semi-structured interview will be used for thematic analysis
Resources (time) needed by the investigators to deliver the intervention3 monthsTime will be used as a measurement tool to quantify total time required to deliver the intervention
Proportion of days with missing nutritional data, as a marker of feasibility3 months
Proportion of adults who fulfils the BMI criteria for recruitment with IT facilities4 weeks

Countries

United Kingdom

Outcome results

None listed

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