跳至主要内容
临床试验/NCT07435610
NCT07435610招募中不适用

A Randomized, Participant- and Assessor-Blinded, Sham-Controlled Trial Investigating Acupuncture for Disorders of Gut-Brain Interaction in Children (P-GAP)

Children's Hospital of Orange County1 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2026年1月8日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
96
试验地点
1

研究概览

简要总结

Disorders of Gut-Brain Interactions (DGBIs) significantly impact children globally, leading to reduced quality of life and increased healthcare utilization. Despite their prevalence, effective treatments for pediatric DGBIs remain limited. Acupuncture, though commonly used in clinical practice and supported by adult data, lacks robust empirical evidence in pediatric populations. This study addresses this critical gap.

The primary objective is to assess the efficacy of acupuncture in reducing symptom severity in pediatric patients with DGBIs. Key secondary objectives include evaluating improvements in quality of life, functional disability, and mental health outcomes.

This is a parallel-group, randomized, placebo sham-controlled, participant-blind clinical trial. The study is being conducted in an outpatient pediatric referral center. A total of 96 participants, aged 8-17 years, meeting eligibility criteria for DGBIs will be enrolled. Participants must be medically stable and meet protocol-defined inclusion/exclusion criteria.

Participants will be randomly assigned to receive either acupuncture or sham acupuncture, alongside standard care. Treatments will occur over a predefined protocol period. Data will be collected at baseline, during treatment, and at specified post-treatment intervals. The primary outcomes will evaluate changes in pain intensity and frequency. Secondary outcomes will include assessments of pain resolution, quality of life, functional disability, and mental health. Statistical analyses will employ rigorous methodologies to ensure reliability and validity of findings.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
8 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Age 8-17 years
  • Diagnosis of FAP-NOS, IBS, or abdominal migraine (Rome IV criteria; partial criteria permitted)
  • Stable use (≥8 weeks) of antidepressant and/or ADHD medications, if applicable
  • Functional constipation, if present, controlled on maintenance therapy
  • Ability of participant and caregiver to comply with study procedures

排除标准

  • Prior treatment with IB-Stim, acupuncture, or other auricular/percutaneous nerve field stimulation modalities.
  • Diagnosis of functional dyspepsia.
  • Untreated constipation at screening.
  • Use of ketamine, opioids, antibiotics, or probiotics within 2 weeks prior to treatment initiation

研究组 & 干预措施

Active

Experimental

The active treatment group will receive standardized acupuncture based on a protocol for functional abdominal pain, using seven acupuncture points: ST36 (Zusanli), LV3 (Taichong), REN12 (Zhongwan), PC6 (Neiguan), SP4 (Gongsun), EX-HN (Sishencong), and DU24 (Shenting) using sterile, single-use Seirin needles. Sessions will occur once weekly for eight weeks, each lasting 40 minutes.

干预措施: Active Therapeutic acupuncture intervention (Other)

Control/Sham

Sham Comparator

The control group will receive Park Sham Acupuncture Devices at the same scalp points, designed to mimic the sensation of acupuncture without actual needle insertion. Both groups will continue receiving standard care throughout the study.

干预措施: Sham therapeutic acupuncture treatment (Other)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ashish Chogle

Principal Investigator

Children's Hospital of Orange County

研究点 (1)

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