EAT-CF: Evaluation of a Behavioural Intervention Using App Technology in CF

Sponsor
Sheffield Teaching Hospitals NHS Foundation Trust (Other)
Overall Status
Completed
CT.gov ID
NCT03782909
Collaborator
(none)
5
1
1
9.8
0.5

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Behaviour change intervention
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
5 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Evaluation of a Behavioural Intervention Using App Technology in Cystic Fibrosis
Actual Study Start Date :
May 8, 2019
Actual Primary Completion Date :
Mar 1, 2020
Actual Study Completion Date :
Mar 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Behaviour change intervention

Intensive behaviour change for 6 weeks, followed by a maintenance phase for 6 weeks

Behavioral: Behaviour change intervention
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

Outcome Measures

Primary Outcome Measures

  1. Proportion of patients who accepted invitation to participate as a marker of feasibility [4 weeks]

Secondary Outcome Measures

  1. Participants' opinion about the behavioural intervention [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 [3 months]

  3. Participants' opinion about the study processes [3 months]

    A semi-structured interview will be used for thematic analysis

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

  6. Resources (time) needed by the investigators to deliver the intervention [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 [3 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years and Older
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust Sheffield South Yorkshire United Kingdom S10 2JF

Sponsors and Collaborators

  • Sheffield Teaching Hospitals NHS Foundation Trust

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sheffield Teaching Hospitals NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT03782909
Other Study ID Numbers:
  • STH20240
First Posted:
Dec 20, 2018
Last Update Posted:
Feb 12, 2021
Last Verified:
Feb 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sheffield Teaching Hospitals NHS Foundation Trust
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 12, 2021