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Feasibility of weekly participant-reported data collection in a pragmatic randomised controlled trial in primary care: experiences from the BATHE trial (Bath Additives for the Treatment of cHildhood Eczema)

Feasibility of weekly participant-reported data collection in a pragmatic randomised controlled trial in primary care: experiences from the BATHE trial (Bath Additives for the Treatment of cHildhood Eczema)
Feasibility of weekly participant-reported data collection in a pragmatic randomised controlled trial in primary care: experiences from the BATHE trial (Bath Additives for the Treatment of cHildhood Eczema)
Background

Patient-reported outcomes measures in clinical trials ensure that evaluations of effectiveness focus on outcomes that are important to patients. In relapsing-remitting conditions, such as eczema, repeated measurements may allow a more accurate reflection of disease burden and treatment effect than less frequent measurements.

We asked parents/carers of children with eczema taking part in a trial of bath emollients to complete weekly questionnaires for 16 weeks.

Methods

The objective of this study was to determine the acceptability and practicality of collecting weekly measures of eczema severity online for 16 weeks in children aged 1 to 11 years as part of the BATHE study.

BATHE randomised patients to bath emollients plus standard eczema care or standard eczema care only. The primary outcome was eczema severity, measured by the seven-item Patient-Oriented Eczema Measure (POEM) repeated weekly for 16 weeks. Acceptability was explored through qualitative interviews with 10 participants. Interviews were audio-recorded, transcribed and analysed thematically. Practicality was assessed by exploring the completeness of the data and keeping a log of any problems.

Results

Four hundred and eighty-two participants were recruited to the trial and 429 opted to complete measures online (89.0%). Data were collected online for 83% of time points over the 16-week period and there was no association between socio-demographic characteristics and data completeness. Two hundred and six (48%) completed their weekly data every week for 16 weeks and 341 (79%) completed it at least 80% of the time. The mean number of weeks completed was 13.3 out of 16 (SD 4.2).

Interviewees said that they understood the rationale behind weekly collection and some welcomed this as it helped them realise how their child’s eczema changed weekly. Whilst some interviewees spoke of weekly questionnaires as onerous, others said that they found them quick and easy. Reminders were welcomed.

Parents/carers seemed happy to receive telephone reminders and it was sometimes useful for eliciting problems relating to obtaining trial medication or password problems for online data collection.

Conclusions

Amongst this population, high levels of data completeness suggests that weekly completion of the online questionnaire appears to be acceptable and feasible over a 16-week period.

Trial registration

ISRCTN84102309. Registered on 9 December 2013.
1745-6215
Stuart, Beth
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Rumsby, Kate
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Santer, Miriam
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Ridd, Matthew
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Francis, Nick
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Chorozoglou, Maria
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Spreadbury, Carla
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Steele, M
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Nollett, Claire
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Liddiard, Lyn
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Prude, Martina
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Hooper, Julie
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Thomas-Jones, Emma
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Roberts, Amanda
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Thomas, Kim
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Williams, Hywel C.
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Little, Paul
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Stuart, Beth
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Rumsby, Kate
2002ee8a-32ac-4119-869d-ed35164c3b51
Santer, Miriam
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Ridd, Matthew
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Francis, Nick
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Chorozoglou, Maria
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Spreadbury, Carla
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Steele, M
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Nollett, Claire
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Liddiard, Lyn
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Prude, Martina
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Hooper, Julie
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Thomas-Jones, Emma
ea15d5ac-8232-4823-ab40-17bec0968520
Roberts, Amanda
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Thomas, Kim
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Williams, Hywel C.
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Little, Paul
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Stuart, Beth, Rumsby, Kate, Santer, Miriam, Ridd, Matthew, Francis, Nick, Chorozoglou, Maria, Spreadbury, Carla, Steele, M, Nollett, Claire, Liddiard, Lyn, Prude, Martina, Hooper, Julie, Thomas-Jones, Emma, Roberts, Amanda, Thomas, Kim, Williams, Hywel C. and Little, Paul (2018) Feasibility of weekly participant-reported data collection in a pragmatic randomised controlled trial in primary care: experiences from the BATHE trial (Bath Additives for the Treatment of cHildhood Eczema). Trials, 19 (1), [582]. (doi:10.1186/s13063-018-2962-3).

Record type: Article

Abstract

Background

Patient-reported outcomes measures in clinical trials ensure that evaluations of effectiveness focus on outcomes that are important to patients. In relapsing-remitting conditions, such as eczema, repeated measurements may allow a more accurate reflection of disease burden and treatment effect than less frequent measurements.

We asked parents/carers of children with eczema taking part in a trial of bath emollients to complete weekly questionnaires for 16 weeks.

Methods

The objective of this study was to determine the acceptability and practicality of collecting weekly measures of eczema severity online for 16 weeks in children aged 1 to 11 years as part of the BATHE study.

BATHE randomised patients to bath emollients plus standard eczema care or standard eczema care only. The primary outcome was eczema severity, measured by the seven-item Patient-Oriented Eczema Measure (POEM) repeated weekly for 16 weeks. Acceptability was explored through qualitative interviews with 10 participants. Interviews were audio-recorded, transcribed and analysed thematically. Practicality was assessed by exploring the completeness of the data and keeping a log of any problems.

Results

Four hundred and eighty-two participants were recruited to the trial and 429 opted to complete measures online (89.0%). Data were collected online for 83% of time points over the 16-week period and there was no association between socio-demographic characteristics and data completeness. Two hundred and six (48%) completed their weekly data every week for 16 weeks and 341 (79%) completed it at least 80% of the time. The mean number of weeks completed was 13.3 out of 16 (SD 4.2).

Interviewees said that they understood the rationale behind weekly collection and some welcomed this as it helped them realise how their child’s eczema changed weekly. Whilst some interviewees spoke of weekly questionnaires as onerous, others said that they found them quick and easy. Reminders were welcomed.

Parents/carers seemed happy to receive telephone reminders and it was sometimes useful for eliciting problems relating to obtaining trial medication or password problems for online data collection.

Conclusions

Amongst this population, high levels of data completeness suggests that weekly completion of the online questionnaire appears to be acceptable and feasible over a 16-week period.

Trial registration

ISRCTN84102309. Registered on 9 December 2013.

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More information

Accepted/In Press date: 3 October 2018
e-pub ahead of print date: 24 October 2018
Published date: 24 October 2018

Identifiers

Local EPrints ID: 425728
URI: http://eprints.soton.ac.uk/id/eprint/425728
ISSN: 1745-6215
PURE UUID: 2f5f4c3e-a8af-4826-a758-e1898c083f01
ORCID for Beth Stuart: ORCID iD orcid.org/0000-0001-5432-7437
ORCID for Kate Rumsby: ORCID iD orcid.org/0000-0002-8573-3718
ORCID for Miriam Santer: ORCID iD orcid.org/0000-0001-7264-5260
ORCID for Nick Francis: ORCID iD orcid.org/0000-0001-8939-7312
ORCID for Maria Chorozoglou: ORCID iD orcid.org/0000-0001-5070-4653
ORCID for Paul Little: ORCID iD orcid.org/0000-0003-3664-1873

Catalogue record

Date deposited: 02 Nov 2018 17:30
Last modified: 12 Jul 2024 02:05

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Contributors

Author: Beth Stuart ORCID iD
Author: Kate Rumsby ORCID iD
Author: Miriam Santer ORCID iD
Author: Matthew Ridd
Author: Nick Francis ORCID iD
Author: Carla Spreadbury
Author: M Steele
Author: Claire Nollett
Author: Lyn Liddiard
Author: Martina Prude
Author: Julie Hooper
Author: Emma Thomas-Jones
Author: Amanda Roberts
Author: Kim Thomas
Author: Hywel C. Williams
Author: Paul Little ORCID iD

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