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Efficacy and Underlying Mechanisms of Group-Based Natural Psychotherapy for Anxiety Disorder

Efficacy and Underlying Mechanisms of Group-Based Natural Psychotherapy for Anxiety Disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07518264
Enrollment
60
Registered
2026-04-08
Start date
2026-03-01
Completion date
2026-07-01
Last updated
2026-07-01

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

Conditions

Obsessive - Compulsive Disorder

Keywords

Obsessive - Compulsive Disorder, Natural Psychotherapy

Brief summary

This study aims to preliminarily explore the intervention effect and feasibility of group natural psychotherapy (a new Eastern culture-based psychotherapy method) for patients with anxiety disorder through a randomized controlled trial.

Detailed description

This study aims to preliminarily explore the intervention effect and feasibility of group natural psychotherapy (a new Eastern culture-based psychotherapy method) for patients with anxiety disorder through a randomized controlled trial. The specific objectives include: 1. Verify the efficacy of group natural psychotherapy: Compare the differences between group natural psychotherapy and conventional treatment in alleviating anxiety and improving the quality of life of patients with anxiety disorder. 2. Evaluate the feasibility of the intervention program: Examine the operability, patient acceptance, and compliance of implementing group natural psychotherapy intervention in a real - clinical environment. 3. Combine cognitive paradigms and functional magnetic resonance imaging (fMRI) technology to explore the cognitive - neural mechanisms of natural psychotherapy in the intervention of anxiety disorder.

Interventions

BEHAVIORALGroup-based Natural Psychotherapy

Patients will be divided into 3-4 groups, with each group comprising 8-10 patients, led by one psychotherapist. The intervention will last 4 weeks, with all patients required to participate in weekly face-to-face group sessions, each lasting 2-3 hours. The weekly group sessions are the core of the treatment and consists of two parts: (1) phase-specific psychoeducation on the theoretical principles of Natural Psychotherapy; (2) experiential learning through carefully designed activities to facilitate personal experience and understanding of the theoretical content. Homework is assigned after each group session, such as writing treatment diaries and daily exercise plans. The psychotherapists review patients' treatment diaries daily according to guiding principles and provide feedback, offering key guidance and support. Exercise is emphasized as a core component of active action within the Natural Psychotherapy; participants will develop personalized weekly exercise plans during group ses

Sponsors

Beijing HuiLongGuan Hospital
Lead SponsorOTHER
Institute of Psychology, Chinese Academy of Sciences
CollaboratorOTHER
Fourth People's Hospital in Hefei
CollaboratorUNKNOWN

Study design

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

Masking description

In the study, primary clinical outcomes were evaluated using self - rating scales.

Eligibility

Sex/Gender
ALL
Age
15 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

1. Meet the diagnostic criteria for anxiety disorders in the DSM - 5; 2. Aged between 15 and 55 years old; 3. Have a junior high school education or above; 4. The patient agrees to participate in this project and signs the informed consent form.

Exclusion criteria

1. Have comorbidities of other severe mental disorders (including schizophrenia, bipolar disorder, and major depressive disorder); 2. Have a lifetime history of substance abuse; 3. Patients with severe neurological diseases, mental retardation, and cognitive impairment; 4. At high risk of suicide or have suicidal behavior; 5. Pregnant or breastfeeding; 6. Have severe physical diseases and infectious diseases.

Design outcomes

Primary

MeasureTime frameDescription
Generalized Anxiety Disorder-7 (GAD-7)week 0; week 4; week 8The GAD-7 is a brief self-report questionnaire designed to assess the severity of generalized anxiety symptoms (Spitzer et al., 2006). It consists of seven items, with higher scores indicating greater severity of anxiety. Clinical cut-off scores are: 0-4 (minimal/no clinical anxiety), 5-9 (mild), 10-14 (moderate), and ≥ 15 (severe). The Chinese version of the GAD-7 has demonstrated good reliability and validity, with high internal consistency (Cronbach's α = 0.93) and satisfactory test-retest reliability (ICC = 0.71-0.87; Zhang et al., 2021).
State-Trait Anxiety Inventory (STAI)week 0; weeek 4; week 8The STAI consists of two subscales (Spielberger et al., 1970): the State Anxiety Inventory (S-Anxiety, Items 1-20) and the Trait Anxiety Inventory (T-Anxiety, Items 21-40). The S-Anxiety subscale reflects transient feelings of tension, apprehension and nervousness in response to stressors, while the T-Anxiety subscale assesses relatively stable individual differences in anxiety proneness. Both subscales use a 4-point Likert scale (total scores 20-80), with higher scores indicating higher levels of anxiety; certain items are reverse-scored. The Chinese version shows robust reliability and validity, with high internal consistency (Cronbach's α = 0.91-0.92), strong test-retest reliability (0.76-0.91), and significant correlations with the HAMA (r = 0.69-0.74; Ma et al., 2012).

Secondary

MeasureTime frameDescription
Intolerance of Uncertainty Scale (IUS)week 0; weeek 4; week 8The IUS is a standard self-report measure for evaluating intolerance of uncertainty (IU). This study uses the 12-item short-form (IUS-12) (Carleton, Sharpe, et al., 2007), which has been validated in Chinese populations (Zhang Y. et al., 2017). Items are rated on a 5-point scale from 0 (not at all characteristic) to 4 (entirely characteristic), with higher total scores indicating higher IU. IUS-12 includes two factors: Prospective IU (Items 1-7) and Inhibitory IU (Items 8-12), though research suggests the total score is a psychometrically sound representation of the construct (Hale et al., 2016; Shihata et al., 2018).
Quality of Life Scale (QOL)week 0; weeek 4; week 8The QOL is a concise self-report tool for assessing individuals' overall quality of life over the past month, emphasizing subjective perceptions across key life domains. The scale comprises 7 items, with the first 6 items evaluating quality of life in physical health, mental and psychological state, economic status, work (or study) situation and interpersonal relationships with family and others, using a 5-point scoring system from "very poor" to "very good" (scored 1-5); these 6 items are summed to obtain the QOL total score. Item 7 is a self-rating of overall quality of life on a 0-100 scale, denoted as QOL score, reflecting individuals' comprehensive evaluation of their overall quality of life.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 2, 2026