Clinical trial Recruiting at 1 site Interventional Ages 8 to 18

Mindfulness for kids with body-focused behaviors

Official title: Mindfulness Intervention and Its Impact on Psychological and Family Dynamics in Children With Body-Focused Repetitive Behaviors.

Run by Children's Hospital of Fudan University · NCT06777212 · Data updated 2026-11-12

This study tests whether a daily mindfulness program helps children aged 8–18 reduce nail-biting, skin-picking, and similar behaviors more than a basic psychosocial education program.

Quick facts

Study typeInterventional
Ages8 Years to 18 Years
SexAll
Enrollment200 (estimated)
SponsorChildren's Hospital of Fudan University
Academic / other
Locations1 site (Shanghai, Shanghai Municipality)
StatusRecruiting
StartedJanuary 1, 2025
Main results expectedDecember 31, 2027
Study endsDecember 31, 2027
Registry record updatedOctober 22, 2026
Trial IDNCT06777212 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are children and adolescents aged 8–18 with observable BFRBs (nail-biting, skin-picking, or hair-pulling) who have not recently received other psychological treatments for BFRBs.

Probably not a fit

Participants currently receiving other psychological or pharmacological treatments for BFRBs, or with conditions that limit participation, may have limited benefit from the mindfulness program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This single-site randomized trial compares a mindfulness training program to a psychosocial education control for children and teens with body-focused repetitive behaviors. Participants follow a 30-day regimen with guided practices and parent involvement, and outcomes include changes in BFRBs and emotional well-being. Standardized assessments will measure behavior frequency, anxiety, and family dynamics to determine if mindfulness offers added benefit. The study is led by the Children’s Hospital of Fudan University in Shanghai and aims to clarify if mindfulness can be a non-pharmacological option for managing BFRBs in youth.

Why it matters

Potential benefit: If successful, the intervention could provide a practical, non-pharmacological option to reduce BFRBs and improve emotional and family well-being.

How similar studies have gone: Previous research suggests mindfulness can help with impulse control and anxiety, supporting potential benefits for BFRBs, though results are variable and more evidence is needed.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:(1)Children and adolescents aged 8 to 18 years. (2)Evidence of significant Body-Focused Repetitive Behaviors (BFRBs) such as nail-biting, skin-picking, or hair-pulling, observed within the last month.

(3)Written informed consent provided by the parent or legal guardian, and child assent provided by the participant.

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Exclusion Criteria:(1)Presence of severe physical illness or neurological disorders that may interfere with participation in the study.

(2)Participants currently receiving psychological interventions or pharmacological treatments for BFRBs or other psychiatric conditions, and who are unable to temporarily discontinue these treatments.

(3)Presence of significant cognitive impairment that would prevent the participant from completing study assessments or interventions.

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Where it's running

  • Children's Hospital of Fudan University
    Shanghai, Shanghai Municipality, China
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.