91̽»¨

Background

In drug trials, researchers record and report the medical harms that participants may experience during a trial. For example, if a participant becomes very unwell or has to go into hospital. It is much less clear on which harms to record and how to identify and report them in trials where interventions try to change behaviour (like stopping smoking, or eating more healthily), Researchers may miss harms that are important to patients or spend lots of time measuring what is not important.   

We have found Behaviour Change Intervention (BCI) trials record harms in different ways or sometimes not at all¹. There is no consistency and so it is hard to compare trials. It is difficult for researchers to decide what they should record and to identify where participants may be being harmed.

¹ Papaioannou, P. et al. (2021) , Journal of Clinical Epidemiology, 136, pp. 64-76

 

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Aims

This study aims to suggest principles or considerations on how to record harms in BCI trials. This will hopefully improve the efficiency, consistency, and transparency of harms recording. 

There are four work packages (WP): 

WP1: Scoping literature review

The  review aims to scope and map the literature to identify definitions, typologies/frameworks of harms, and suggested principles for recording harms in BCI trials .

WP2: Qualitative interviews with experts 

To elicit perspectives and experiences of CTU and NIHR investigators involved in designing and delivering BCI trials. This will be done through focus groups and individual interviews with multi-disciplinary experts delivering NIHR trials. Topics will include views on purpose or need for monitoring harms in BCI trials, perspectives on how adverse event (AE) recording should be undertaken, problems during implementation of AE data collection and interpretation. 

WP3: Workshops

It was originally planned to conduct a two-stage online Delphi survey and consensus meeting. However, following the interviews in WP2, it was decided with the Project Steering Committee that clear, concise statements could not be developed and would likely result in findings from an online Delphi study that were difficult to interpret. 

Instead, the findings from WP1 and WP2 were used to develop a guidance document for CTU staff and other investigators on how to identify and record harms in BCI trials.

Multi-disciplinary CTU staff, NIHR investigators and Patient and Public Involvement (PPI) members were invited to an online workshop to review the draft guidance. 

WP4: Suggested principles and considerations for harms recording 

Recommendations and an explanatory guidance document for AE recording in BCI trials will be developed These will be made available on the project website.

RHABIT Project Protocol Version 2.0 (Word, 168KB)

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Project timelines 

This project commenced on 1 October 2021.

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Funding

This study has been funded through NIHR CTU Support funding.

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Study team

Contact us at rhabit@sheffield.ac.uk

This project is a collaboration between four UK CRC Clinical Trials Units: 91̽»¨, Nottingham, Cardiff and Imperial.