Assessing the feasibility of injectable growth-promoting therapy in Crohn's disease
Mabrouka A Altowati1, Ashley P Jones2, Helen Hickey2
1Developmental Endocrinology Research Group, University of Glasgow, Scotland, UK ; Department of Paediatric Gastroenterology, Royal Hospital for Sick Children, Glasgow, UK.
Insights
Nearly half of children with Crohn's disease and their parents are willing to join a growth-promoting therapy trial. Addressing injection fears could improve recruitment for this important pediatric Crohn's disease study.
Area of Science:
- Pediatric Gastroenterology
- Clinical Trial Feasibility
- Growth Disorders
Background:
- Crohn's disease (CD) frequently causes growth retardation in children, even with optimal treatment.
- Investigating novel therapies for growth promotion in pediatric CD is crucial.
Purpose of the Study:
- To assess the feasibility of a randomized control trial (RCT) for injectable growth-promoting therapy in children with CD.
- To survey the attitudes of children with CD and their parents towards participating in such an RCT.
Main Methods:
- A feasibility study determined trial parameters including sample size and eligible patient numbers.
- Face-to-face questionnaires assessed willingness to consent to a future RCT among children with CD (HtSDS ≤+1) and their parents.
- 94 out of 118 (80%) questionnaires were returned.
Main Results:
- The study included 94 children with a median age of 14.3 years and a median HtSDS of -1.2.
- 47% of children and 46% of parents were willing to participate in the RCT.
- Fear of injections was a major barrier (44%), while willingness increased among children concerned about their height (61% slightly concerned, 100% very concerned).
Conclusions:
- Approximately half of surveyed children with CD and their parents expressed willingness to join an RCT for growth-promoting therapy.
- Addressing and alleviating fears related to injections could significantly enhance recruitment rates for future trials.
Background:
Despite optimal therapy, many children with Crohn's disease (CD) experience growth retardation. The objectives of the study are to assess the feasibility of a randomised control trial (RCT) of injectable forms of growth-promoting therapy and to survey the attitudes of children with CD and their parents to it.
Methods:
A feasibility study was carried out to determine study arms, sample size and numbers of eligible patients. A face-to-face questionnaire surveyed willingness to consent to future participation in the RCT. Eligibility to the survey was any child under 18 (with their parent/guardian) with CD whose height standard deviation score (HtSDS) was ≤+1. Of 118 questionnaires, 94 (80%) were returned (48 by children and 46 by parents).
Results:
The median age of the patients in the survey was 14.3 years (range 7.0 to 17.7), and 35 (73%) were male. Their median HtSDS was -1.2 (-3.01, 0.23), and it was lower than the median mid-parental HtSDS of -0.6 (-3.1, 1.4). We analysed the willingness of the children whose HtSDS <-1 to take part in the proposed RCT, being those most likely to require treatment. Overall, 18 (47%) children and 17 (46%) parents were willing. This increased to 61% of children who were slightly concerned about their height and 100% (4/4) of those very concerned. A common reason for not taking part in the RCT was fear of injections (44%); 111 children are required for randomisation into three study arms from nine centres.
Conclusions:
Almost half of children and parents surveyed would take part in an RCT of growth-promoting therapy. Allaying fears about injections may result in higher recruitment rates.
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