跳至主要内容
临床试验/NCT03813901
NCT03813901已完成不适用

Advaita Vedanta and Counselling for Women Who Have Experienced Intimate Partner Violence: Impact on Women's Health

NMP Medical Research Institute2 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2018年6月21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
入组人数
102
试验地点
2
主要终点
Change in Quality of Life

研究概览

简要总结

Violence has immediate effects on women's health, which in some cases, is fatal. Physical, mental and behavioural health consequences can also persist long after the violence has stopped. Violence against women and girls occurs in every country and culture and is rooted in social and cultural attitudes and norms that privilege men over women and boys over girls.

Research consistently finds that the more severe the abuse, the greater its impact on women's physical and mental health. In addition, the negative health consequences can persist long after abuse has stopped.Present work shares the impact of arsha vidya counselling for women who has been victim of violence.

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
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Able to attend regular counselling
  • Planning to remain in area for next 6 months
  • have experience intimate partner violence (physical, emotional, psychological, and/or sexual), including coercive control from a current or former partner in the previous 12 months and no later than 3 years.

排除标准

  • Under 19 years of age
  • Cannot attend at regular basis
  • Living outside of the selected study sites, or planning to relocate in next 4 months
  • Separated more than 3 years ago

研究组 & 干预措施

Samalochana Counselling group

Experimental

Arsha Vidya advaita vedanta based counselling were given to the women

干预措施: Samalochana Counselling (Other)

Wait-list control group

Other

Wait list group were not given any supportive care during the period. After that, they were offered the similar program as Counselling group.

干预措施: Wait list control (Other)

结局指标

主要结局

Change in Quality of Life

时间窗: Change from baseline to 12-week

Quality of Life was measured using SF-36 questionnaire

次要结局

  • Change in Anxiety(Change from Baseline to 12-weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验