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临床试验/NCT07153653
NCT07153653招募中不适用

Effect of Baduanjin Exercise Intervention on Pregnancy-Related Pain and Quality of Life: A Randomized Controlled Trial

Peking Union Medical College Hospital1 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2025年3月13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
84
试验地点
1
主要终点
Low Back Pain Severity

研究概览

简要总结

This is a randomized controlled trial studying whether a 12-week Baduanjin exercise program (a traditional Chinese mind-body exercise) can reduce low back pain and improve quality of life in pregnant women.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Single pregnancy (carrying one fetus).
  • •Gestational age: 14-20 weeks at enrollment.
  • •No contraindications to exercise during pregnancy (as determined by medical evaluation).

排除标准

  • •Adverse pregnancy symptoms:
  • •Dizziness, blurred vision, vaginal bleeding, or other high-risk signs.
  • •Pre-existing medical conditions: Orthopedic, cardiovascular, or psychiatric diseases; cognitive impairment.
  • •Pregnancy complications: Preterm labor, placenta previa.
  • •Inability to attend regular prenatal check-ups.

研究组 & 干预措施

Baduanjin Group

Experimental

Prenatal Baduanjin Exercise Program

干预措施: Prenatal Baduanjin Exercise Program (Behavioral)

Standard Clinic Prenatal Care

No Intervention

结局指标

主要结局

Low Back Pain Severity

时间窗: Baseline, 6 weeks, post-intervention (12 weeks)

Measured using Numerical Rating Scale (NRS) where 0 = no pain and 10 = worst imaginable pain. Assesses self-reported low back/pelvic girdle pain intensity.

次要结局

  • Back Disability(Baseline, 6 weeks, post-intervention (12 weeks))
  • Urinary Incontinence(Baseline, 6 weeks, post-intervention (12 weeks))
  • Pelvic Disability(Baseline, 6 weeks, post-intervention (12 weeks))
  • Urinary Incontinence Severity(Baseline, 6 weeks, post-intervention (12 weeks))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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