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临床试验/NCT07764042
NCT07764042已完成不适用

Investigation of the Effects of Wet Cupping Therapy on Immune Modulation, Pulmonary Function, and Quality of Life in Patients With Asthma

Medipol University1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2025年5月19日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
52
试验地点
1
主要终点
Change in FVC From Baseline to 2 Months

研究概览

简要总结

This study evaluated the effects of wet cupping therapy on immune modulation, pulmonary function, and quality of life in adults with asthma. A total of 52 participants aged 30 to 55 years were allocated to either a control group or a wet cupping therapy group. Participants in the wet cupping therapy group received two sessions of wet cupping therapy, at baseline and one month later. Participants in both groups underwent clinical assessments at baseline and at two months. Pulmonary function, asthma-related quality of life, asthma control, dyspnea, fatigue, anxiety, and depression were assessed in both groups. Selected inflammatory markers were assessed only in the wet cupping therapy group.

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
None

入排标准

年龄范围
30 Years 至 55 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adults aged 30 to 55 years.
  • •Clinically diagnosed with asthma.
  • •Asthma diagnosis established at least 6 months before enrollment.
  • •No wet cupping therapy within the previous 2 months.
  • •No herbal supplementation affecting asthma within the previous 2 months.
  • •Able to cooperate with spirometry testing.

排除标准

  • •Presence of another chronic disease.
  • •Hospitalization during the study period.

研究组 & 干预措施

Control Group

No Intervention

Participants in the control group underwent pulmonary function testing at baseline and at two months and completed the study assessment scales at baseline and at the end of the study.

Wet Cupping Therapy Group

Experimental

Participants received wet cupping therapy twice during the two-month study period, with the first session at baseline and the second session one month later. Pulmonary function testing and study assessments were performed at baseline and at two months.

干预措施: Wet Cupping Therapy (Procedure)

结局指标

主要结局

Change in FVC From Baseline to 2 Months

时间窗: Baseline and 2 months

Forced vital capacity (FVC) was assessed by spirometry. Change from baseline to 2 months was evaluated.

Change in Asthma Quality of Life Questionnaire Score From Baseline to 2 Months

时间窗: Baseline and 2 months

Asthma-related quality of life was assessed using the Asthma Quality of Life Questionnaire (AQLQ). Higher scores indicate better asthma-related quality of life.

Change in COPD and Asthma Fatigue Scale Score From Baseline to 2 Months

时间窗: Baseline and 2 months

Fatigue was assessed using the COPD and Asthma Fatigue Scale. Higher scores indicate greater fatigue severity.

Change in FEV1 From Baseline to 2 Months

时间窗: Baseline and 2 months

Forced expiratory volume in 1 second (FEV1) was assessed by spirometry. Change from baseline to 2 months was evaluated.

Change in FEV1/FVC Ratio From Baseline to 2 Months

时间窗: Baseline and 2 months

The FEV1/FVC ratio was assessed by spirometry. Change from baseline to 2 months was evaluated.

Change in PEF From Baseline to 2 Months

时间窗: Baseline and 2 months

Peak expiratory flow (PEF) was assessed by spirometry. Change from baseline to 2 months was evaluated.

Change in Systemic Immune-Inflammation Index (SII) in the Wet Cupping Therapy Group From Baseline to 2 Months

时间窗: Baseline and 2 months

The Systemic Immune-Inflammation Index (SII) was calculated from peripheral blood cell counts using platelet, neutrophil, and lymphocyte values. SII was assessed only in the wet cupping therapy group. The change in SII from baseline to 2 months was evaluated as an indicator of systemic immune-inflammatory status.

Change in Systemic Inflammation Response Index (SIRI) in the Wet Cupping Therapy Group From Baseline to 2 Months

时间窗: Baseline and 2 months

The Systemic Inflammation Response Index (SIRI) was calculated from peripheral blood cell counts using monocyte, neutrophil, and lymphocyte values. SIRI was assessed only in the wet cupping therapy group. The change in SIRI from baseline to 2 months was evaluated as an indicator of systemic inflammatory status.

次要结局

  • Change in Asthma Control Test Score From Baseline to 2 Months(Baseline and 2 months)
  • Change in Modified Medical Research Council Dyspnea Scale Score From Baseline to 2 Months(Baseline and 2 months)
  • Change in Hospital Anxiety and Depression Scale Scores From Baseline to 2 Months(Baseline and 2 months)
  • Change in Eosinophil Level in the Wet Cupping Therapy Group From Baseline to 2 Months(Baseline and 2 months)

研究者

发起方
Medipol University
申办方类型
Other
责任方
Principal Investigator
主要研究者

TUBA ÖZDEMİR

Family Medicine Specialist

Medipol University

研究点 (1)

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