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NCT Number: NCT03782909

Evaluation of a Behavioural Intervention Using App Technology in CF

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.

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Key information

Age range

16 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust

Sheffield, South Yorkshire, S10 2JF, United Kingdom

Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

Behaviour change intervention

Behavioral

The behaviour change intervention consists of;

  • Feedback via an app based food diary
  • 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

Primary outcomes

  1. Proportion of patients who accepted invitation to participate as a marker of feasibility

    Time frame: 4 weeks

Secondary outcomes

  1. Participants' opinion about the behavioural intervention

    Time frame: 3 months

    A semi-structured interview will be used for thematic analysis

  2. Participant attrition rate and phases of the study whereby the attrition occurs

    Time frame: 3 months

  3. Participants' opinion about the study processes

    Time frame: 3 months

    A semi-structured interview will be used for thematic analysis

  4. Participants' suggestions for further improvement of the intervention and study processes

    Time frame: 3 months

    A semi-structured interview will be used for thematic analysis

  5. Proportion of adults who fulfils the BMI criteria for recruitment with IT facilities

    Time frame: 4 weeks

  6. Resources (time) needed by the investigators to deliver the intervention

    Time frame: 3 months

    Time will be used as a measurement tool to quantify total time required to deliver the intervention

  7. Proportion of days with missing nutritional data, as a marker of feasibility

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

Sheffield Teaching Hospitals NHS Foundation Trust

Other

Registry information

Official study title

Evaluation of a Behavioural Intervention Using App Technology in Cystic Fibrosis

Acronym: EAT-CF

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Dec 20, 2018
Registry last updated
Feb 12, 2021

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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