NCT07201779
Adaptation of REDCHIP Intervention for the Portuguese Context
Not Yet Recruiting · Not Applicable · ISPA - Instituto Universitario de Ciencias Psicologicas, Sociais e da Vida · registry updated 2025-10-01
Inclusion and exclusion lines below are quoted from ClinicalTrials.gov. No match score is shown, because a score needs a person's age, biomarkers, and treatment dates. Confirm the record with the study team.
The present Feasibility Randomized Controlled Trial (FRCT) aims to assess the acceptability and effectiveness of REDCHiP intervention, targeting parents of young children with T1D, followed in two major Portuguese hospitals. The objective of this trial is to evaluate (1) acceptability and feasibility by evaluating recruitment and retention rates, attendance throughout the sessions, and responses to parent satisfaction; (2) effectiveness by analyzing changes in parents' FH, diabetes distress (DD), emotional regulation (ER), resilient coping skills (RC), and anxiety and depression as well as changes in child glycemic outcomes (HbA1c, GMI, TBR, TIR, TAR) at three time points among participants allocated on intervention versus Treatment As Usual (TAU) group. Finally, (3) the investigators aim to qualitatively evaluate participant´s experiences and feedback regarding the REDHIP intervention through interviews.
Inclusion
- Primary caregivers must have a young child aged ≤ 8 years with a confirmed diagnosis of T1D for at least three months;
- Young children must be using either an continuous subcutaneous insulin infusion (CSII) or multiple daily insulin injections (MDI) and continuous glucose monitoring (CGM) for daily T1D treatment;
- Parents must have internet access and a computer, tablet or smartphone that connects to the internet.
Exclusion
- Parents with severe psychiatric diagnosis;
- Families of children with another severe chronic condition (e.g., chronic kidney disease and Crohn's disease);
- Parents who are not fluent in Portuguese.