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临床试验/CTRI/2022/05/042599
CTRI/2022/05/042599招募中2 期

Development and evaluation of women centric comprehensive weight management module

Department of science and technology DST0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Group A: Postpartum women
  • i. Women aged between 25-35 years.
  • ii. Women in the postpartum period from 6 weeks to 6 months post-delivery, after
  • 37 week pregnancy term through a normal or C-section delivery.
  • iii. Women who gave singleton birth.
  • iv. BMI between >= 25 to <=39.9kg/m2.
  • v. Women who can provide a history of pre-pregnancy weight and gestational
  • weight gain (3, 6 and 9 months) as medical record or recall.
  • vi. Women who can read in Hindi/ English.
  • vii. Women who will be lactating.
  • Group B: Perimenopausal women
  • i. Menopausal women aged between 40-55 years.
  • ii. Women with an intact uterus, >= 1 functioning ovary and >=1 menstrual period in past 12
  • iii. BMI between >= 26 to <=39.9kg/m2.
  • iv. Women who can read in Hindi/ English.
  • v. Intend to follow up regularly will be included in the study.
  • vi. The ownership or accessibility to mobile phones for technology based intervention.

排除标准

  • Group A: Postpartum women
  • i) Women with pregnancy related complications (pre-eclampsia, pre-term, hemorrhage, infection).
  • ii) Patients with secondary causes of obesity (like Hypothyroidism, Cushingâ??s
  • diseases, PCOS).
  • iii) Acute infections, advanced end-organ damage or chronic diseases: renal/ hepatic
  • failure, any malignancy
  • iv) Current intake of medicine known to affect body weight such as drugs acting on
  • the central nervous system, cathartics, thyroid supplements, diuretics and selective
  • serotonin reuptake inhibitors.
  • v) Psychosocial contraindications such as bulimia nervosa, anorexia nervosa,
  • substance abuse, clinically significant depression or under current psychiatric
  • Group B: Perimenopausal women
  • i. Women using oral or injectable hormonal contraception, tamoxifen, tibolone and
  • raloxifene in the previous 3 months.
  • ii. Patients with secondary causes of obesity (like Hypothyroidism, Cushingâ??s diseases,
  • iii. Acute infections, advanced end-organ damage or chronic diseases: renal/ hepatic failure,
  • any malignancy.
  • iv. Current intake of medicine known to affect body weight such as drugs acting on the
  • central nervous system, cathartics, thyroid supplements, diuretics and selective serotonin
  • reuptake inhibitors.
  • v.Psychosocial contraindications such as bulimia nervosa, anorexia nervosa, substance abuse, clinically significant depression or under current psychiatric care.
  • vi. Planning to move out within the study period

研究者

发起方
Department of science and technology DST

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Women centric weight management module | 临床试验