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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06950905
Enrollment
122
Registered
2025-04-30
Start date
2025-06-18
Completion date
2028-06-30
Last updated
2025-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Health, Self Concept, Body Dissatisfaction, Compassion, Self-Perception, Mindfulness Meditation, Meditation, Psychological Well-being

Keywords

Feeding Your Demons, Self-Deconstruction, Selflessness, Contemplative Practices, Meditation, Compassion, Body Image, Women's Mental Health, Randomized Controlled Trial (RCT), mindfulness, psychological well-being

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.

Detailed description

Feeding Your Demons (FYD) is a secular contemplative practice inspired by the Tibetan Buddhist tradition, integrating elements of mindfulness, compassion, and symbolic visualization. The practice offers a guided process through which individuals face internal difficulties-referred to as demons-and transform them through acceptance and self-compassion. This study aims to evaluate the effectiveness of FYD compared to a mindfulness meditation intervention. It is a randomized controlled trial (RCT) with two parallel groups. A total of 122 adult women will participate. Participants will be randomly assigned to either the FYD group or the control group. Both interventions will be delivered online over eight weeks. Variables assessed include psychological well-being, body image, body acceptance, mindfulness, compassion, and self-deconstruction. Assessments will be conducted before and after the intervention, and at a six-month follow-up. Statistical analyses will include intra- and intergroup comparisons using repeated measures analysis of variance. Parametric or non-parametric tests will be applied depending on the assumptions met. Relationships between variables will also be analyzed through correlations. Effect sizes will be calculated to estimate the magnitude of observed changes. The significance level will be set at p \< .05, with a 95% confidence interval. This study adopts a mixed-methods approach, combining quantitative assessments with qualitative interviews conducted with a subgroup of participants. Although the data are collected complementarily, their analysis and dissemination may be conducted separately or integratively, depending on the specific goals of each research phase.

Interventions

BEHAVIORALFeeding your demons practice

The Feeding Your Demons (FYD) is a contemplative practice based on the Tibetan Buddhist tradition, adapted in a secular form. The intervention is online and lasts a total of 8 weeks. During this period, participants will engage in weekly home practice of the FYD method using guided audio. The intervention includes 3 expert-facilitated sessions: an initial individual session, a group session at week 4, and a final group session at week 8.

The control group will undergo an online mindfulness meditation intervention, lasting a total of 8 weeks. It includes 3 expert-facilitated sessions: an initial individual session, a group session at week 4, and a final group session at week 8. Participants will engage in weekly home practice of mindfulness meditation using guided audio.

Sponsors

Hospital Miguel Servet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
30 Years to 60 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Delusion of Me Index (DoM)From baseline to 6-month follow-upThe primary outcome will be the change in self-related perception from baseline to 6-month follow-up after randomisation. This includes changes in acceptance, decentering, and non-attachment. Participants will complete this measure at three time points: baseline (week 0), post-intervention (week 8), and 6-month follow-up.
Body Shape Questionnaire-10 (BSQ-10)From baseline to 6-month follow-upThe second primary outcome will be the change in body image from baseline to 6-month follow-up after randomisation. This includes reductions in negative body image, specifically body dissatisfaction. Participants will complete this measure at three time points: baseline (week 0), post-intervention (week 8), and 6-month follow-up.
Body Appreciation Scale-2 (BAS-2)From baseline to 6-month follow-upThe second primary outcome will be the change in body image from baseline to 6-month follow-up after randomisation. This includes improvements in positive body image, specifically body appreciation. Participants will complete this measure at three time points: baseline (week 0), post-intervention (week 8), and 6-month follow-up.
Nondual Awareness Dimensional Assessment (NADA)From baseline to 6-month follow-upThe primary outcome will be the change in self-related perception from baseline to 6-month follow-up after randomisation. This outcome includes changes in nondual awareness. Participants will complete this measure at three time points: baseline (week 0), post-intervention (week 8), and 6-month follow-up.

Secondary

MeasureTime frameDescription
SOCS-S Sussex-Oxford Self- Compassion ScaleFrom baseline to 6-month follow-upChange in Self - Compassion
Five Facet Mindfulness Questionnaire (FFMQ).From baseline to 6-month follow-upChange in Mindfulness
Pemberton Happiness Index (PHI)From baseline to 6-month follow-upChange in Psychological Well- Being
Body Image Acceptance and Action Questionnaire (BI-AAQ-5).From baseline to 6-month follow-upChange in Body Acceptance
Sussex- Oxford Compassion Scale (SOCS - O)From baseline to 6-month follow-upChange in Compassion (for others)
Multidimensional Assessment of Interoceptive Awareness (MAIA)From baseline to 6-month follow-upChange in Interoceptive Awareness

Other

MeasureTime frameDescription
Place of ResidenceAt baselineThe place of residence (e.g., community or city) of participants will be recorded at baseline.
Prior Meditation ExperienceAt baselineParticipants will report whether they have prior meditation experience (yes/no) and, if applicable, the number of months or years of practice.Additionally, they will indicate the type of meditation practice previously performed (e.g., mindfulness, compassion, other).
Employment StatusAt baselineEmployment status (e.g., employed, unemployed, student) will be collected at baseline.
Education LevelAt baselineParticipants will report their highest completed education level at baseline.
Number of Meditation SessionDuring the 8-week interventionParticipants will indicate the sequential number of each formal meditation session completed during the 8-week intervention (e.g., Session 1, Session 2, Session 3).
Perceived Quality of Meditation PracticeDuring the 8-week interventionAfter each formal meditation session, participants will rate the perceived quality of their practice on a scale from 0 (very poor) to 10 (excellent).
Self-reported Affective State after PracticeDuring the 8-week interventionParticipants will rate their affective state immediately after each formal meditation session on a scale from 0 (very negative) to 10 (very positive).
Qualitative phenomenological explorationFrom baseline to post-intervention (8 weeks after baseline)Semi-structured micro-phenomenological interviews will be conducted at baseline and immediately after the 8-week intervention to explore participants' lived experience related to self-perception, embodiment, and contemplative transformation. These data are exploratory and will not be included in inferential statistical analyses.
Participant AgeAt baselineAge of participants, measured in years.

Countries

Spain

Contacts

Primary ContactJavier Garcia Campayo
investigaprimaria@gmail.com976 50 65 78

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026