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Pilot Study of Behavioural Intervention for Nutrition in Cystic Fibrosis

Pilot Study of Behavioural Intervention for Nutrition in Cystic Fibrosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01957072
Acronym
PIN-CF
Enrollment
17
Registered
2013-10-08
Start date
2014-02-28
Completion date
2014-12-31
Last updated
2015-03-11

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

Conditions

Cystic Fibrosis

Keywords

Cystic fibrosis, 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 lung infections and reduced nutrients absorption from food. The average age at death is 26 years, usually from respiratory failure. Nonetheless, the nutritional status of people with CF (PWCF) is important help them live healthier and longer. It is recommended that adult with CF achieve a BMI of 23 for males and 22 for females. However, fewer than 50% adult with CF achieved that target BMI despite effective nutritional support to help support 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. 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 the how many people are needed for the larger trial. All eligible 75 PWCF in Sheffield will be invited to participate. The investigators anticipate recruiting 30 participants. Participants will be divided into two groups. The first group receive the behavioural intervention immediately. The second group receive the intervention after 3 months. All participants will be followed up for 6 months. Data will be collected every 6 weeks during clinic reviews. These two groups will be compared against each other to estimate the potential impact of the behavioural intervention. The investigators will also interview some of the participants at the end of the study period to improve the intervention and the study processes based on participant feedback. The investigators hypothesised that this study will recruit around 30 participants, around 80% of the participants will complete the study, a single full-time investigator can deliver the intervention to 15 participants over 3 months and data collection will be thorough (with less than 5% missing data). The investigators also hypothesised that this feasibility study will help improve the intervention and help the design of a larger trial.

Interventions

The behaviour change intervention consists of 1. feedback via a web-based food diary 2. 'coaching' with problem-solving and implementation plans The intensive intervention phase consists of 2 home visits, 8 telephone calls and 6 reminder emails. The maintenance phase consists of 3 telephone calls and 4 reminder emails.

Sponsors

Sheffield Teaching Hospitals NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
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 Unit * best BMI of \< 23 for males and \< 22 for females between Oct '12 and Oct '13

Exclusion criteria

* patients in the palliative phase of disease * patients who are pregnant * patients who have no capacity to consent to participate in the study * patients who have no IT facilities to use the web-based food diary * 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
Proportion of people with CF who are randomised into the study after accepting the invitation to participate, as a marker of feasibility4 weeks

Secondary

MeasureTime frameDescription
Participants' opinion about the study processes6 months
Participants' suggestions for further improvement of the intervention and study processes6 months
Proportion of adults who fulfils the BMI criteria for recruitment with IT facilities2 weeks
Resources needed by the investigators to deliver the intervention6 months
Proportion of days with missing nutritional data, as a marker for feasibility6 monthsParticipants are requested to fill in their nutritional intake daily on a web-based food diary. The investigators are interested to find out what the proportion of such data will be missing to determine the feasibility of collecting data with the web-based food diary.
Participants' opinion about the behavioural intervention6 months
Participant attrition rate and phases of study whereby the attrition occurs6 months

Other

MeasureTime frameDescription
Weight6 monthsunit is kg
Body mass index6 monthsUnit is kg/m2
The mean Self-Report Behavioural Automaticity Index (SRBAI) score6 monthsAs a marker of habit formation
Beliefs about Medicines Questionnaire (BMQ) score6 monthsAs a marker of patients' perception of their treatment

Countries

United Kingdom

Outcome results

None listed

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