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Recruiting NCT06950905

NCT06950905 Contemplative Practice for Well-being and Self-Deconstruction in Women

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Clinical Trial Summary
NCT ID NCT06950905
Status Recruiting
Phase
Sponsor Hospital Miguel Servet
Condition Mental Health
Study Type INTERVENTIONAL
Enrollment 122 participants
Start Date 2025-06-18
Primary Completion 2026-06-30

Eligibility & Interventions

Sex Female only
Min Age 30 Years
Max Age 60 Years
Study Type INTERVENTIONAL
Interventions
Feeding your demons practiceMindfulness practice

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 122 participants in total. It began in 2025-06-18 with a primary completion date of 2026-06-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This randomized controlled trial aims to evaluate the effectiveness of a contemplative practice called Feeding Your Demons (FYD), based on a secular adaptation of Tibetan Buddhism, in improving psychological well-being, body image, body acceptance, compassion, and self-deconstruction in adult women. Participants will be randomly assigned to either FYD or an active control group practicing mindfulness meditation. Psychological variables will be assessed before and after the intervention, and at a six-month follow-up. Additionally, a qualitative exploration will be conducted through interviews with a subgroup of participants.

Eligibility Criteria

Inclusion Criteria: * Sex assigned female at birth and self-identifies as a woman * Aged between 30 and 60 years * Spanish nationality, or residency in Spain for more than 5 years * Fluent in Spanish * At least one month of experience with meditation or mindfulness practices, with a regular practice of more than 15 minutes per session * Provides informed consent Exclusion Criteria: * Indicators of eating disorders (ED) or mental health deterioration, determined by the following cut-off points: SCOFF ≥ 2 and PHQ-9 ≥ 10 * Formal diagnosis of an eating disorder or any psychiatric condition * Substance use disorder * History of neurological disease diagnosis * Participant's decision to withdraw from the study at any point

Contact & Investigator

Central Contact

Javier Garcia Campayo

✉ investigaprimaria@gmail.com

📞 976 50 65 78

Frequently Asked Questions

Who can join the NCT06950905 clinical trial?

This trial is open to female participants only, aged 30 Years or older, up to 60 Years, studying Mental Health. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06950905 currently recruiting?

Yes, NCT06950905 is actively recruiting participants. Contact the research team at investigaprimaria@gmail.com for enrollment information.

Where is the NCT06950905 trial being conducted?

This trial is being conducted at Zaragoza, Spain, Zaragoza, Spain.

Who is sponsoring the NCT06950905 clinical trial?

NCT06950905 is sponsored by Hospital Miguel Servet. The trial plans to enroll 122 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology