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临床试验/NCT01429636
NCT01429636已完成3 期

Phase 3 Study of Applied Relaxation (AR) Technique That Treating Menopausal Symptoms

Chiang Mai University2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2011年8月最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
60
试验地点
2
主要终点
Changes in global scores of Menopausal Rating Scale (MRS).

研究概览

简要总结

The purpose of this study is to demonstrate better efficacy and effectiveness of modified applied relaxation technique over its original version for treating menopausal symptoms.

详细描述

Applied Relaxation (AR) is the most commonly used behavioral methods for treating menopausal symptoms. Many clinical trials reported that the technique effectively improved vasomotor and related symptoms. There is a strong evidence to support its continue use in clinical settings.

However, the original AR technique is too cumbersome. It involves intensive training once a week for 12 consecutive weeks. Each weekly session takes 60 minutes, and subjects are requested to do self-practice at home for at least 15-20 minutes/day. As such, >25% of recruited subjects drop out from the training course. The investigators have modified the original AR technique by reducing the duration of training to only once, lasting 60 minutes. Participants are requested to do self-practice at home for 15-20 minutes/day as in the original technique. Instead of coming to a weekly class, the investigators use telephone to communicate with the subjects once a week for 12 consecutive weeks. A preliminary study showed all 10 recruited subjects remained in the study (MR; modified relaxation technique) until completion. They all reported dramatic improvement in their vasomotor symptoms.

In this study, the investigators propose to compare our modified version of AR with the original method in a randomized controlled clinical trial. The subjects will be Thai menopausal women with vasomotor symptoms. The main outcomes are the reduction in the MRS score (intensity of hot flushes, night sweats and sleep disturbances) among those who remain in the program at the end of the study (efficacy evaluation). As nearly all patients will remain in the MR group, while >25% of those in the AR group will be expected to drop out from the study, the investigators should be able to demonstrate a superiority of MR over AR in terms of effectiveness as well.

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
45 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Perimenopausal women and postmenopausal women with either surgical or spontaneous menopause.
  • Women who have at least 5 points of MRS score.

排除标准

  • Women who are taking any hormone therapy for any reason in the past three months prior to entering the trails.
  • Women with uncontrolled hypertension (>95mmHg diastolic pressure) or daily use of sedatives, tranquilizer or antidepressant medication.

结局指标

主要结局

Changes in global scores of Menopausal Rating Scale (MRS).

时间窗: 12 weeks

MRS measure after intervention at 1, 2 and 3 months for follow-up.

次要结局

  • Change in the frequency and severity of hot flushes.(12 weeks)
  • Change in the frequency and severity of night sweats.(12 weeks)
  • Change in the frequency and severity of sleep disturbances.(12 weeks)

研究者

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

Suprawita Saensak

Phase 3 Study of Applied Relaxation (AR) Technique versus Its Modified Version for Treating Menopausal Symptoms.

Chiang Mai University

研究点 (2)

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