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ABOUT
Trial Forge Centres
WHAT’S NEW?
Improving Trial Diversity
Making trials more accessible through better patient information leaflets
How to consider sex and gender in trials
Working with diverse ethnic communities
How to decide which ethnic groups your trial needs
How to collect ethnicity data
The INCLUDE Ethnicity Framework
Common design considerations when involving particular ethnic groups in trials
How to include people with impaired capacity to consent in trials
The INCLUDE Impaired Capacity to Consent Framework
How to include socioeconomically disadvantaged people in trials
The INCLUDE Socioeconomic Disadvantage Framework
How to include older people in health and social care research
How to apply a trauma and resilience-informed approach in trials
Intersectionality: looking beyond single identities to make trials more inclusive
PRO EDI: improving how equity, diversity and inclusion are handled in trials and evidence synthesis
RESOURCES
SWAT Resources
Protocols and resources for priority recruitment and retention SWATs (PRESS)
Library of participant information leaflets (EXCELSIOR)
Principles for handling end-of-participation events in trials (PeRSEVERE)
TOUR DATES
PUBLICATIONS
PATHWAY
ABOUT
Trial Forge Centres
WHAT’S NEW?
Improving Trial Diversity
Making trials more accessible through better patient information leaflets
How to consider sex and gender in trials
Working with diverse ethnic communities
How to decide which ethnic groups your trial needs
How to collect ethnicity data
The INCLUDE Ethnicity Framework
Common design considerations when involving particular ethnic groups in trials
How to include people with impaired capacity to consent in trials
The INCLUDE Impaired Capacity to Consent Framework
How to include socioeconomically disadvantaged people in trials
The INCLUDE Socioeconomic Disadvantage Framework
How to include older people in health and social care research
How to apply a trauma and resilience-informed approach in trials
Intersectionality: looking beyond single identities to make trials more inclusive
PRO EDI: improving how equity, diversity and inclusion are handled in trials and evidence synthesis
RESOURCES
SWAT Resources
Protocols and resources for priority recruitment and retention SWATs (PRESS)
Library of participant information leaflets (EXCELSIOR)
Principles for handling end-of-participation events in trials (PeRSEVERE)
TOUR DATES
PUBLICATIONS
PATHWAY
Search
ABOUT
Trial Forge Centres
WHAT’S NEW?
Improving Trial Diversity
Making trials more accessible through better patient information leaflets
How to consider sex and gender in trials
Working with diverse ethnic communities
How to decide which ethnic groups your trial needs
How to collect ethnicity data
The INCLUDE Ethnicity Framework
Common design considerations when involving particular ethnic groups in trials
How to include people with impaired capacity to consent in trials
The INCLUDE Impaired Capacity to Consent Framework
How to include socioeconomically disadvantaged people in trials
The INCLUDE Socioeconomic Disadvantage Framework
How to include older people in health and social care research
How to apply a trauma and resilience-informed approach in trials
Intersectionality: looking beyond single identities to make trials more inclusive
PRO EDI: improving how equity, diversity and inclusion are handled in trials and evidence synthesis
RESOURCES
SWAT Resources
Protocols and resources for priority recruitment and retention SWATs (PRESS)
Library of participant information leaflets (EXCELSIOR)
Principles for handling end-of-participation events in trials (PeRSEVERE)
TOUR DATES
PUBLICATIONS
PATHWAY
ABOUT
Trial Forge Centres
WHAT’S NEW?
Improving Trial Diversity
Making trials more accessible through better patient information leaflets
How to consider sex and gender in trials
Working with diverse ethnic communities
How to decide which ethnic groups your trial needs
How to collect ethnicity data
The INCLUDE Ethnicity Framework
Common design considerations when involving particular ethnic groups in trials
How to include people with impaired capacity to consent in trials
The INCLUDE Impaired Capacity to Consent Framework
How to include socioeconomically disadvantaged people in trials
The INCLUDE Socioeconomic Disadvantage Framework
How to include older people in health and social care research
How to apply a trauma and resilience-informed approach in trials
Intersectionality: looking beyond single identities to make trials more inclusive
PRO EDI: improving how equity, diversity and inclusion are handled in trials and evidence synthesis
RESOURCES
SWAT Resources
Protocols and resources for priority recruitment and retention SWATs (PRESS)
Library of participant information leaflets (EXCELSIOR)
Principles for handling end-of-participation events in trials (PeRSEVERE)
TOUR DATES
PUBLICATIONS
PATHWAY
Trial Forge on tour: presentations and talks
Please Select Year
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
5
Oct
2017
Update to the Cochrane review of trial recruitment interventions
Speaker:
Shaun Treweek |
Location:
Liverpool, UK
Read More…
18
Sep
2017
Precisely how can this tool help investigators design trials
Speaker:
Shaun Treweek, Heidi Gardner |
Location:
Cape Town, South Africa
Read More…
14
Sep
2017
Strategies to improve participant recruitment to randomised controlled trials
Speaker:
Heidi Gardner |
Location:
Cape Town, South Africa
Read More…
14
Sep
2017
The inefficiency of isolation: why evidence providers and evidence synthesisers can break out of their silo
Speaker:
Heidi Gardner |
Location:
Cape Town, South Africa
Read More…
14
Sep
2017
Strategies to improve participant recruitment to randomised controlled trials
Speaker:
Heidi Gardner |
Location:
Cape Town, South Africa
Read More…
15
Aug
2017
Talking Science
Speaker:
Heidi Gardner |
Location:
Aberdeen, UK
Read More…
17
Jul
2017
Trial Forge: helping to make trials more efficient
Speaker:
Shaun Treweek |
Location:
Health Research Authority, London, UK
Read More…
26
Jun
2017
Making trials more efficient: Trial Forge and how you can help
Speaker:
Shaun Treweek |
Location:
Oxford, UK
Read More…
21
Jun
2017
Routinely collected health data (RCD) for randomised controlled trials
Speaker:
Lars Hemkens & Heidi Gardner |
Location:
Oxford, UK
Read More…
20
Jun
2017
Efficiency in clinical trials
Speaker:
Shaun Treweek |
Location:
Aberdeen, UK
Read More…
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