Actively Recruiting

Phase Not Applicable
Age: 12Years - 18Years
All Genders
NCT07138417

Compassion-Based Family Intervention for Adolescents

Led by Beijing HuiLongGuan Hospital · Updated on 2026-05-08

60

Participants Needed

1

Research Sites

95 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Adolescents with emotional disorders (such as depression or anxiety) often experience distress that also affects their parents, creating a cycle of stress within the family. This study tests a new compassion-based family intervention designed to help both adolescents and their parents. The program includes six weekly sessions (120 minutes each). The study will recruit 60 parent-adolescent dyads. Half will receive the intervention immediately; the other half will wait 6 weeks before receiving it. We will measure changes in depression, anxiety, parenting stress, family relationships, and - using brain imaging (fNIRS) and heart rate monitors - how the intervention affects parent-child emotional and physiological synchrony. Assessments will take place before the intervention, right after, and at 3-month and 6-month follow-ups. The goal is to see whether this family-focused compassion program can improve mental health for both adolescents and their parents.

CONDITIONS

Official Title

Compassion-Based Family Intervention for Adolescents

Who Can Participate

Age: 12Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adolescent aged 12 to 18 years
  • Adolescent has a Hamilton Depression Rating Scale (HAMD-17) total score between 17 and 30, or a Hamilton Anxiety Rating Scale (HAMA) total score between 18 and 29
  • The item 3 score (suicide) of HAMD-17 for the adolescent is 2 or less
  • At least one parent is willing to participate
  • Adolescent has normal hearing, vision, and intellectual abilities
  • Participating parent has normal reading and writing skills
  • Adolescent has no history of manic episodes
Not Eligible

You will not qualify if you...

  • Adolescent has psychotic symptoms, bipolar disorder, or schizophrenia
  • Parent has a mental illness or psychological disorder
  • Adolescent or parent has a history of substance abuse
  • Adolescent or parent has a severe neurological disorder or major physical disease
  • Adolescent or parent is assessed as having a high suicide risk

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hefei Fourth People's Hospital (Anhui Mental Health Center; Affiliated Psychological Hospital of Anhui Medical University)

Hefei, Anhui, China, 230022

Actively Recruiting

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Research Team

D

Dongmei Wang, Ph.D

CONTACT

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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