Pilot Study of Behavioural Intervention for Nutrition in Cystic Fibrosis (PIN-CF)
Primary Purpose
Cystic Fibrosis
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Behaviour change intervention
Sponsored by
About this trial
This is an interventional health services research trial for Cystic Fibrosis focused on measuring Cystic fibrosis, Nutrition, Weight, BMI, Behaviour change
Eligibility Criteria
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
Sites / Locations
- Northern General Hospital, Sheffield Teaching Hospitals NHS Foundation Trust
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Behaviour change intervention
Wait-list Control
Arm Description
Intensive behaviour change intervention for 3 months, followed by a maintenance phase for 3 months
Usual care for 3 months, followed by intensive behaviour change intervention for 3 months
Outcomes
Primary Outcome Measures
Proportion of patients who accepted invitation to participate as a marker of feasibility
Proportion of people with CF who are randomised into the study after accepting the invitation to participate, as a marker of feasibility
Secondary Outcome Measures
Participants' opinion about the behavioural intervention
Participant attrition rate and phases of study whereby the attrition occurs
Participants' opinion about the study processes
Participants' suggestions for further improvement of the intervention and study processes
Proportion of adults who fulfils the BMI criteria for recruitment with IT facilities
Resources needed by the investigators to deliver the intervention
Proportion of days with missing nutritional data, as a marker for feasibility
Participants 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.
Full Information
NCT ID
NCT01957072
First Posted
September 30, 2013
Last Updated
March 10, 2015
Sponsor
Sheffield Teaching Hospitals NHS Foundation Trust
1. Study Identification
Unique Protocol Identification Number
NCT01957072
Brief Title
Pilot Study of Behavioural Intervention for Nutrition in Cystic Fibrosis
Acronym
PIN-CF
Official Title
Pilot Study of Behavioural Intervention for Nutrition in Cystic Fibrosis
Study Type
Interventional
2. Study Status
Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sheffield Teaching Hospitals NHS Foundation Trust
4. Oversight
Data Monitoring Committee
No
5. 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 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis
Keywords
Cystic fibrosis, Nutrition, Weight, BMI, Behaviour change
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
17 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Behaviour change intervention
Arm Type
Experimental
Arm Description
Intensive behaviour change intervention for 3 months, followed by a maintenance phase for 3 months
Arm Title
Wait-list Control
Arm Type
Other
Arm Description
Usual care for 3 months, followed by intensive behaviour change intervention for 3 months
Intervention Type
Behavioral
Intervention Name(s)
Behaviour change intervention
Intervention Description
The behaviour change intervention consists of
feedback via a web-based food diary
'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.
Primary Outcome Measure Information:
Title
Proportion of patients who accepted invitation to participate as a marker of feasibility
Time Frame
4 weeks
Title
Proportion of people with CF who are randomised into the study after accepting the invitation to participate, as a marker of feasibility
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Participants' opinion about the behavioural intervention
Time Frame
6 months
Title
Participant attrition rate and phases of study whereby the attrition occurs
Time Frame
6 months
Title
Participants' opinion about the study processes
Time Frame
6 months
Title
Participants' suggestions for further improvement of the intervention and study processes
Time Frame
6 months
Title
Proportion of adults who fulfils the BMI criteria for recruitment with IT facilities
Time Frame
2 weeks
Title
Resources needed by the investigators to deliver the intervention
Time Frame
6 months
Title
Proportion of days with missing nutritional data, as a marker for feasibility
Description
Participants 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.
Time Frame
6 months
Other Pre-specified Outcome Measures:
Title
Body mass index
Description
Unit is kg/m2
Time Frame
6 months
Title
Weight
Description
unit is kg
Time Frame
6 months
Title
Beliefs about Medicines Questionnaire (BMQ) score
Description
As a marker of patients' perception of their treatment
Time Frame
6 months
Title
The mean Self-Report Behavioural Automaticity Index (SRBAI) score
Description
As a marker of habit formation
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martin J Wildman, PhD
Organizational Affiliation
Sheffield Teaching Hospitals NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northern General Hospital, Sheffield Teaching Hospitals NHS Foundation Trust
City
Sheffield
State/Province
South Yorkshire
ZIP/Postal Code
S5 7AU
Country
United Kingdom
12. IPD Sharing Statement
Learn more about this trial
Pilot Study of Behavioural Intervention for Nutrition in Cystic Fibrosis
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