CompletedNot Applicable

Intervention in Chronic Pediatric Patients and Their Families.

Spain500 participantsStarted 2019-02-04

Plain-language summary

This project consists of a psychological intervention in patients and their families with different chronic diseases in order to carry out a comparative study between medical pathologies to know which are the protective or risk variables for the adaptation to the disease.

Who can participate

Age range

12 Years – 16 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Diagnosis at least 6 months. * To have signed the informed consent. Exclusion Criteria: * No previous psychological diagnosis. * Attention Deficit Hyperactivity Disorder(ADHD), epilepsy or brain tumor * Infant cerebral palsy * Not understanding the Spanish language

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Change Emotional Distress in caregivers (Baseline-Pre-Post)

Timeframe: Baseline up to 12 months

Change Emotional Distress in patients (Baseline-Pre-Post)

Timeframe: Baseline up to 12 months

Change Caregiver burden (Baseline-Pre-Post)

Timeframe: Baseline up to 12 months

Change Emotional competences in patients (Baseline-Pre-post)

Timeframe: Baseline up to 12 months

Change Self-esteem in patients (Baseline-Pre-Post)

Timeframe: Baseline up to 12 months

Change of Perceived level of disease threat (Baseline-Pre-Post)

Timeframe: Baseline up to 12 months

Trial details

NCT IDNCT04476433

SponsorUniversity of Valencia

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-12-30

View on ClinicalTrials.gov More Type 1 Diabetes trials

Who can participate

Age range

12 Years – 16 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Change Emotional Distress in caregivers (Baseline-Pre-Post)

Timeframe: Baseline up to 12 months

Change Emotional Distress in patients (Baseline-Pre-Post)

Timeframe: Baseline up to 12 months

Change Caregiver burden (Baseline-Pre-Post)

Timeframe: Baseline up to 12 months

Change Emotional competences in patients (Baseline-Pre-post)

Timeframe: Baseline up to 12 months

Change Self-esteem in patients (Baseline-Pre-Post)

Timeframe: Baseline up to 12 months

Change of Perceived level of disease threat (Baseline-Pre-Post)

Timeframe: Baseline up to 12 months