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ADAPT: Acceptability of online dietary assessment of irritable bowel syndrome (IBS) patients in clinical practice

A randomised controlled trial to evaluate the feasibility of web-based dietary assessment for improved personalised dietary advice in routine clinical dietetic practice of irritable bowel syndrome (IBS) patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12932938
Enrollment
80
Registered
2022-01-06
Start date
2022-06-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Irritable bowel syndrome (IBS) Digestive System

Interventions

A sample between 80 and 100 patients diagnosed with IBS will be randomly allocated (1:1) to web-based 24-hour dietary recalls or routine dietetic practice (dietary history interview method) and follow

Sponsors

Cambridge University Hospitals NHS Foundation Trust
Lead Sponsor
University of Cambridge
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Newly admitted patients older than 18 years 2. Meet the ROME IV criteria for IBS diagnosis according to the National Institute for Health and Care Excellence (NICE) guidelines

Exclusion criteria

Exclusion criteria: 1. Younger than 18 years 2. Co-existing gastrointestinal disease (e.g. inflammatory bowel disease, celiac disease) or eating disorder 3. No availability or access to a computer, tablet, or internet 4. Insufficient English language proficiency 5. Unable to give informed consent

Design outcomes

Primary

MeasureTime frame
IBS adequate relief and symptom severity score measured by IBS symptoms questionnaire at baseline, monthly, within 2 weeks pre-dietetic appointment, discharge and end of study time points.

Secondary

MeasureTime frame
1. Adherence to dietetic advice - measured by IBS symptoms questionnaire at baseline, monthly, within 2 weeks pre-dietetic appointment, discharge and end of study time points. 2. Quality of dietetic practice - measured by Satisfaction, acceptability and Quality of Care questionnaire at the discharge timepoint. Also measured using information from CUH electronic medical notes at at baseline, monthly, within 2 weeks pre-dietetic appointment, discharge and end of study time points. 3. Response rates and acceptability of dietary assessment methods - measured by Satisfaction, acceptability and Quality of Care questionnaire at the discharge timepoint. 4. Quality of life (IBS specific) - measured by IBS Quality of Life questionnaire at baseline, discharge and end of study timepoints. 5. Dietetic consultation time (for one-to-one consultations only) - measured using information from CUH electronic medical notes at at baseline, monthly, within 2 weeks pre-dietetic appointment, discharge and end of study time points. 6. Frequency of follow-up dietetic consultations (for one-to-one consultations only) - measured using information from CUH electronic medical notes at at baseline, monthly, within 2 weeks pre-dietetic appointment, discharge and end of study time points.

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026