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RCT Protocol: Emotion Regulation for Eco Anxiety & Eating Concerns in Mexicans Adults

NCT07536243 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2026-04-17

No results posted yet for this study

Summary

The goal of this clinical trial is to evaluate the effect of a group intervention based on emotion regulation as a coping strategy for eco-anxiety and eating-related eco-concerns in Mexican adults. The main questions it aims to answer are:

* Does the intervention group show a significant decrease in eco-anxiety at the end of the intervention and at the four-month follow-up?
* Does the intervention group show a significant reduction in eating-related eco-concerns, as well as improvement in emotion regulation and adaptive coping styles?

Researchers will compare the intervention group with the control group to determine whether an intervention based on emotion regulation improves adaptive coping styles.

Participants will:

* Attend the intervention sessions weekly for 6 weeks.
* Complete the assessment instruments at three time points: prior to the start of the intervention, at the end of the intervention, and 4 months post-intervention.

Conditions

  • To Evaluate the Effect of a Group Intervention Based on Emotion Regulation

Interventions

OTHER

Emotional Regulation for Eco Anxiety & Eating Concerns

The program consists of six 90-minute sessions. Each session will be led by a psychologist with expertise in CBT and group interventions, accompanied by a support psychologist with experience in group settings who will be present throughout all sessions. Each session follows this structure: welcome, mindfulness exercise, development of a coping strategy, at-home practice activity, and closing

Sponsors & Collaborators

  • University of Washington

    collaborator OTHER

  • Universidad de San Martín de Porres (USMP)

    collaborator UNKNOWN

  • Universidad Veracruzana

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
59 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-04-20
Primary Completion
2026-05-28
Completion
2026-09-28

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07536243 on ClinicalTrials.gov