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临床试验/NCT06921174
NCT06921174招募中2 期

Comparison of the Effectiveness of Classical Perineal Massage Therapy Versus the Use of an Intravaginal Device to Reduce Postpartum Perineal Pain

Instituto Sexológico Murciano1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2025年3月27日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
140
试验地点
1
主要终点
Visual Analogue Scale (VAS) - to assess pain intensity

研究概览

简要总结

GA34.01 postpartum, a randomized design with a parallel group structure will be applied, randomly assigning participants into two groups. The first group will receive the traditional perineal massage therapy, while the second group will use the intravaginal device "Crescendo 2." In this study, a pre- and post-intervention evaluation will be conducted, using the Visual Analog Scale (VAS) as the primary outcome measure and the Clinical Global Impression Scale as the secondary outcome measure.

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 (Participant, Care Provider)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Women aged 18 years or older.
  • •Residing in the Region of Murcia.
  • •Having had a vaginal delivery between 6 weeks and 12 months prior to enrollment.
  • •Presenting postpartum perineal pain, coded in ICD-11 as GA34.
  • •Have not received any prior treatment for this condition.

排除标准

  • •Presence of severe conditions such as:
  • •Excessive postpartum hemorrhage
  • •Serious infections
  • •Respiratory or circulatory complications
  • •Neurological disorders requiring intensive medical intervention
  • •Currently under pharmacological treatment for pelvic pain.
  • •Active vaginal infections.
  • •Expressed refusal to participate or inability to comply with study procedures.
  • •Women with episiotomy may participate only if there were no complications such as severe infection or hemorrhage following the procedure.
  • •Willingness to participate and to follow the study protocol.
  • •Exclusion Criteria:

研究组 & 干预措施

Use of the "Crescendo 2" Intravaginal Device

Experimental

Self-administered perineal massage at home.

Three times per week, 10 minutes each session, over a 12-week period.

干预措施: Use of the "Crescendo 2" Intravaginal Device (Device)

Classical Perineal Massage Therapy

Active Comparator

Performed manually by a pelvic floor physiotherapist.

One 30-minute session per week for 12 weeks.

干预措施: Classical Perineal Massage Therapy (Procedure)

结局指标

主要结局

Visual Analogue Scale (VAS) - to assess pain intensity

时间窗: First measure week 1 and Last measure week 12

The \*\*Visual Analogue Scale (VAS)\*\* will be used as the \*\*primary outcome measure\*\*. It consists of a horizontal line approximately 10 centimeters long. At each end of the line are the extreme expressions of pain: on the left, "no pain," and on the right, "worst imaginable pain." This tool allows us to measure the intensity of pain with high reproducibility between observers. Visual Analogue Scale (VAS): The Visual Analogue Scale is a psychometric response scale used to measure pain intensity. It typically consists of a 10-centimeter horizontal line anchored by two verbal descriptors: "no pain" (score = 0) and "worst imaginable pain" (score = 10). Minimum score: 0 (no pain) Maximum score: 10 (worst imaginable pain) Interpretation: Higher scores indicate worse outcomes (i.e., more intense pain).

次要结局

  • Clinical Global Impression (CGI) - for overall health status(At the end of the treatment week 12)

研究者

发起方
Instituto Sexológico Murciano
申办方类型
Other
责任方
Sponsor

研究点 (1)

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