Comparing Acupuncture With Medication to Reduce Anxiety and Depression in China

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorDuke Kunshan University

About this trial

The main objective of this study is to compare medication (usual care) with acupuncture (as a standalone comparator) to identify the most (cost)effective and environmentally sustainable intervention to reduce anxiety and mild to moderate depression in adults in China.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Chinese nationals 18 years old and above

No mental health treatment in the past 6 months

Depressive disorder (F30-F39)

Fear anxiety disorder (F40)

Disqualifiers

Serious cardiovascular, cerebrovascular, liver, kidney and other serious life-threatening primary diseases

Poorly controlled diabetes

There is a risk of suicide

Those with head trauma, loss of consciousness or severe mental disorders

Trial design

Design model

Parallel

Treatments tested in this trial

  • Selective serotonin reuptake inhibitor (SSRI)

    Drug

    This pharmacological intervention (selective serotonin reuptake inhibitor (SSRI)) will be compared to acupuncture (for which no drugs will be involved). Treatment options for medication will be determined by the medical team, the usual care recommended for patients diagnosed with anxiety and depression. Treatment is expected to last 1 month per patient. Expected treatment plan: Administer Toludesvenlafaxine (40-80 mg daily) or imported Sertraline (50-200 mg daily), supplemented with Lorazepam (0.4-0.8 mg) or Alprazolam (0.4-0.8 mg) as needed for sleep support.

  • Acupuncture

    Other intervention

    Manual acupuncture (no sham) will be compared to medication. Bilateral Baihui (GV20), Yintang (GV29), Shenmen (HT7), Taichong (LR3), Neiguan (PC6), Sanyinjiao (SP6), and Zusanli (ST36). Procedure: 1. Positioning: The patient lies in a supine position. 2. Needles: Disposable sterile acupuncture needles (specification: 0.25 mm × 40 mm, brand: Wuxi Jiajian) are used. 3. Sterilization: Strict disinfection is performed before needle insertion. 4. Needling Technique: After insertion, lifting-thrusting and twisting techniques are applied to achieve deqi\* (needling sensation). 5. Retention Time: Needles are retained for 20 minutes. 6. Treatment Schedule: * Sessions per week: 3 times. * Course duration: 9-10 sessions per treatment course. Detailed Needling Methods for Each Acupoint Acupoint Location Needling Insertion Technique and Depth Baihui (GV20) On the head, 5 cun\* directly above the midpoint of the anterior hairline. Horizontal insertion to a depth of 0.5-0.8 c

Treatment groups

120 Participants
are divided into 2 treatment groups
Group A: Selective serotonin reuptake inhibitor (SSRI)Experimental treatment 1 intervention
Group B: AcupunctureActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Between-groups and within-subjects mean change in depression

Changes in depression will be measured with Patient Health Questionnaire-9 (PHQ-9). The PHQ-9 is a versatile tool for screening, diagnosing, monitoring, and assessing depression severity. The prompt instruction is: Over the last 2 weeks, how often have you been bothered by any of the following problems? Example of items: "Little interest or pleasure in doing things"; "Feeling down, depressed, or hopeless". Scoring options include: 0=not at all, 1=several days, 2=more than half of the days, 3=nearly every day. Lower mean values suggest aggregate reductions in depression.

Time frame
Collected at baseline T0, after intervention T1 (after 3-4 weeks intervention), and at 3-month follow-up T2.
2

Between-groups and within-subjects mean change in anxiety

Change in anxiety will be measured with the Generalised Anxiety Disorder Assessment (GAD-7). GAD-7 is a brief measure for symptoms of anxiety, based on the generalised anxiety disorder (GAD) diagnostic criteria described in the Diagnostic and Statistical Manual of Mental Disorders (DSM). The prompt instruction is: Over the last 2 weeks, how often have you been bothered by any of the following problems? Example of items: "Feeling nervous, anxious, or on edge"; "Not being able to stop or control worrying". Scoring options include: 0=not at all, 1=several days, 2=more than half of the days, 3=nearly every day. Lower mean values suggest aggregate reductions in anxiety.

Time frame
Collected at baseline T0, after intervention T1 (after 3-4 weeks intervention), and at 3-month follow-up T2.

Secondary outcomes

1

Between-groups Comparative Environmental Footprint

To calculate the comparative environmental impacts of acupuncture versus antidepressants to reduce postpartum depression, we will consider a range of factors including list of resources, quantities used (e.g., electricity, water), emissions factors and indirect emissions e.g., supply chain. We will follow validated calculation methods for healthcare, which will allow to identify, measure and evaluate the total emission impacts of different health treatments. This calculation will document all resources used in both arms of the trial, including medications, acupuncture materials, travel, infrastructure use (e.g., clinic space), and any other resources engaged during the trial. Both treatments have waste that must be managed. We will normalize the footprint data per patient or per unit of clinical improvement to facilitate a direct comparison between the two treatments. The final single, combined value will be reported as CO2 emissions in tonnes.

Time frame
After treatment is concluded (Time 1) and 3-months follow-up (Time 2)
2

Between-groups Comparative Cost-Effectiveness

To conduct a cost-effectiveness analysis, we will delineate all direct and indirect costs associated with interventions, including treatment session fees, medication costs, healthcare professional time, and travel expenses for patients. Incremental cost-effectiveness ratios (ICERs) will be calculated by comparing the difference in mean costs to the difference in mean effectiveness between the two treatments, with effectiveness measured in quality-adjusted life years (QALYs) gained, derived from validated, condition-specific health-related quality of life measures. A decision-analytic model will be employed to extrapolate trial results to a longer time horizon, and sensitivity analyses involving varying key parameters will be used to assess the robustness of the results and account for uncertainty in the trial data and model projections.

Time frame
After treatment is concluded (Time 1) and at 3-months follow-up (Time 2)

Other outcomes

1

Between-groups and within-subjects mean change in Side Effects

Participants will be asked to rate the frequency of possible side effects. The prompt instruction is: How often have you been bothered by these problems in the last 2 weeks? Nausea; Headache; Tremor/ shaking hands; Heart palpitations; Constipation; Dizziness; Indigestion; Pain; Insomnia; Fatigue. Scoring options include: 0=not at all, 1=several days, 2=more than half of the days, 3=nearly every day. Lower values suggest lower rates of side effects.

Time frame
Collected at baseline T0, after intervention T1 (after 3-4 weeks intervention), and at 3-month follow-up T2.
2

Alcohol Use Rate

Alcohol use rate will be evaluated with the Alcohol Use Disorders Identification Test (AUDIT-C). One question: How often do you have a drink containing alcohol? From Never (0), Monthly or less (1), 2-4 month (2), 2-3 times per week (3) to 4+ times per week (4).

Time frame
Collected at baseline T0, after intervention T1 (after 3-4 weeks intervention), and at 3-month follow-up T2.
3

Smoking Rate

Smoking rate will be measured with the Cigarette Dependence Scale short version (CDS). The CDS scale will ask e.g., On average, how many cigarettes do you smoke per day? From zero (0) I don't smoke to 30+ (5).

Time frame
Collected at baseline T0, after intervention T1 (after 3-4 weeks intervention), and at 3-month follow-up T2.
4

Between-groups and within-subjects mean change in Social Media Addiction

The Bergen Social Media Addiction Scale (BSMAS) will be used to evaluate mean changes in online use behavior. This scale comprises six items based on the six core components (salience, mood, modification, tolerance, withdrawal conflict and relapse) e.g., "Use a lot of time thinking about or planning using social media"), and smartphone apps addiction (e.g., "My smartphone is the most important thing in my life"). The six items are responded to using a five-point Likert type scale ranging between 1 (very rarely) and 5 (very often). A higher score in the BSMAS indicates a greater likelihood of being at risk of developing a social media addiction.

Time frame
Collected at baseline T0, after intervention T1 (after 3-4 weeks intervention), and at 3-month follow-up T2.

Sponsors and contacts

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Duke Kunshan University

Lead sponsor

Kunshan Hospital of Traditional Chinese Medicine

Collaborator

Kunshan Mental Health Center

Collaborator

National Natural Science Foundation of China

Collaborator

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