Actively Recruiting

Phase Not Applicable
Age: 30Years - 60Years
FEMALE
ID06950905

Effectiveness of a Contemplative Practice on Psychological Well-Being, Self-Deconstruction, Body Image, Body Acceptance, and Compassion in Women

Led by Hospital Miguel Servet · Updated on 2025-09-10

122

Participants Needed

2

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating 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 aged 30 to 60. This randomized controlled trial compares FYD with an active control group practicing mindfulness meditation, aiming to understand how these practices impact mental and emotional health. The study includes 122 women fluent in Spanish, with prior meditation experience. Participants will be randomly assigned to either the FYD or mindfulness meditation group. Both interventions are delivered online over eight weeks, involving weekly home practice sessions guided by audio. Each group receives three expert-led sessions: an initial individual meeting, a group session at week 4, and a final group session at week 8. The FYD practice involves a structured process of identifying internal challenges and transforming them through acceptance and compassion, while the mindfulness group focuses on breath awareness and non-judgmental observation. Participants will complete assessments before and after the intervention, and again at a six-month follow-up. These include psychological measures such as the Delusion of Me Index, Body Appreciation Scale, and various questionnaires on mindfulness, self-compassion, and body acceptance. A subgroup will also take part in qualitative interviews. Researchers will analyze changes over time and relationships between variables to understand the effects of both practices on well-being, compassion, and self-perception.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 30Years - 60Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • Indicators of eating disorders or mental health deterioration (SCOFF 6 2 and PHQ-9 6 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

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or online)

Outpatient Treatment

Duration - 8 weeks

Participants engage in an online contemplative practice or mindfulness meditation lasting 8 weeks, including weekly home practice and three expert-facilitated sessions: an initial individual session, a group session at week 4, and a final group session at week 8.

3 expert-facilitated sessions (online) plus weekly home practice

Follow-up

Duration - 6 months

Participants are assessed to measure the lasting effects of the intervention at 6 months after completing the treatment.

1 follow-up assessment (online or in-person)

Trial Site Locations

Total: 2 locations

1

Department of Psychiatry. Miguel Servet University Hospital

Zaragoza, Zaragoza, Spain, 50009

Not Yet Recruiting

2

University of Zaragoza

Zaragoza, Zaragoza, Spain, 50009

Actively Recruiting

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Research Team

J

Javier Garcia Campayo

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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