Clinic Recruitment for Cluster RCT

Overview of the D1 Now Definitive Trial

The D1 Now Definitive Trial is a groundbreaking research study aimed at improving self-management and clinical engagement among young adults with Type 1 diabetes (T1D). This trial seeks to evaluate the effectiveness and cost-effectiveness of the D1 Now intervention, a comprehensive approach designed to support young adults during a crucial period of their lives as they navigate the complexities of managing T1D.

Why This Study Matters

Addressing Unique Challenges

Managing T1D during young adulthood presents unique challenges, including poor glycaemic control and increased risk of complications.

Supporting Transitions

The D1 Now intervention provides targeted support to help young adults navigate life transitions while managing their condition.

Enhancing Patient-Clinician Communication

This study fosters better communication between patients and clinicians, improving self-management practices.

Trial Design and Methodology

Phase 1: Recruitment

Recruitment of 348 participants across 12 centres.

Phase 2: Implementation

Participants will be randomized into intervention and usual care groups.

Phase 3: Monitoring

Continuous monitoring of HbA1c levels and other health outcomes.

Phase 4: Analysis

Data analysis to evaluate the effectiveness of the D1 Now intervention.

Benefits of Participation

Contribute to valuable research that could transform diabetes care.
Receive structured support and resources.
Enhance patient care and clinical engagement.

Frequently Asked Questions

Will previous involvement in the pilot affect recruitment?

Most previous participants have likely aged out of the target group, and we are focusing on reaching a broader population this time, including those who may not currently attend regular clinic appointments.

Can centres already using an agenda-setting tool participate?

Yes, centres can continue with their current agenda-setting tools. This study aims to complement existing practices, and we will include an item in our survey to describe the current usual care.

What support will be provided?

Each centre in the intervention arm will receive a trial coordinator and a support worker. These roles are flexible, ensuring they are available when needed, and they will be trained to assist with participant recruitment, data collection, and implementation of the intervention.