跳至主要内容
临床试验/CTRI/2025/09/094151
CTRI/2025/09/094151招募中不适用

Effect of a twenty-minute brisk walk on symptoms of generalized anxiety disorder, in addition to pharmacological treatment—A randomized controlled trial

Konaseema Institute of Medical sciences and research foundation1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2025年9月30日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
120
试验地点
1
主要终点
The primary outcome will be assessed by the Hamilton Anxiety Rating Scale.

研究概览

简要总结

Anxiety disorders manifest across the lifespan and are characterized by excessive symptoms of fear and anxiety over a prolonged period, accompanied by behavioural changes and non-specific physiological arousal. It results in significant distress, functional impairment, disability, diminishment of educational and economic potential, and lowered quality of life. It is the world’s most common mental disorder, affecting 301 million people in 2019.  Women are more affected by anxiety disorders than men. Approximately 1 in 4 people with anxiety disorders receive treatment for this condition. The current prevalence of anxiety disorders (including PTSD and OCD) in India is 2.94%, according to the National Mental Health Survey 2016. Brisk walking is a moderate-intensity aerobic exercise, characterized by a faster pace than a stroll, typically around 3 miles per hour (or 100 steps per minute), and it raises your heart rate and breathing. Previous studies have demonstrated that moderate exercise, like brisk walking, improves depression, anxiety, and mental health in individuals. In the present study, we aimed to find the association between brisk walking and anxiety disorders among adults.

Brisk walking for 20 minutes as a lifestyle modification will be advised over pharmacological treatment in one group, while the other group will receive purely pharmacological treatment. Compliance with brisk walking was assessed by giving a semi-structured self-reporting questionnaire to participants. The anxiety symptoms at baseline will be assessed using the Hamilton Anxiety Rating Scale (HAM-A) and repeated at the end of 2 weeks and 4 weeks. The assessor will be blinded to which group the participants belong.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Subjects who are newly diagnosed with Generalised anxiety disorder according to ICD-
  • 18-65 years of age 3) Patients who have given informed consent 4) Patients who have a sedentary lifestyle.

排除标准

  • People who were already doing physical activities 2) Any chronic physical illness 3) Any severe comorbid psychiatric illness.

结局指标

主要结局

The primary outcome will be assessed by the Hamilton Anxiety Rating Scale.

时间窗: at baseline, at 2 weeks and 4 weeks

次要结局

未报告次要终点

研究者

发起方
Konaseema Institute of Medical sciences and research foundation
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

K Ramya Krishna

Konaseema Institute of Medical Sciences and Reseach foundation

研究点 (1)

Loading locations...

相似试验