跳至主要内容
临床试验/NCT05260112
NCT05260112已完成不适用

Implementation of a Text Message and Multimedia-based Program for Women Newly Diagnosed With Interstitial Cystitis/Bladder Pain Syndrome

University of Pennsylvania1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2021年11月5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
52
试验地点
1
主要终点
Change in Pain Self Efficacy Scale

研究概览

简要总结

To implement and assess clinical efficacy of a text message and multimedia-based program that (i) remotely delivers first- and second-line American Urological Association (AUA) treatments of IC/BPS; (ii) integrates treatment of biological (neuropathic pain, pelvic floor dysfunction), psychological (symptom-related fear and anxiety) and social (barriers in access to care, limited patient-provider communication) domains of IC/BPS; (iii) uses clinically validated messages to provide guidance and support.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

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 over 18
  • •AUA (American Urological Association) criteria for IC/BPS of "an unpleasant sensation (pain, pressure, discomfort) perceived to be related to the urinary bladder, associated with lower urinary tract symptoms of more than six weeks duration, in the absence of infection or other identifiable causes"
  • •Interested in first- or second-line AUA treatment
  • •Negative urinalysis and culture within two months of enrollment
  • •English-speaking
  • •Own a smartphone with text message and video viewing capability

排除标准

  • •Women currently on third line or higher treatments
  • •Currently being treated for UTI
  • •History of voiding dysfunction such as urinary retention or neurogenic bladder
  • •Recent (<6 months) pelvic surgery/pregnancy
  • •Prior pelvic malignancy or radiation

研究组 & 干预措施

ERICA

Experimental

ERICA is a smartphone-based educational program that teaches women newly diagnosed with interstitial cystitis evidence-based strategies to self-manage their symptoms at home. The program is designed to bridge the interval/gap between initial visit where they are diagnosed with interstitial cystitis and follow up visit. Participants received video learning modules via a secure and HIPAA-compliant text messaging system.

干预措施: ERICA (Other)

结局指标

主要结局

Change in Pain Self Efficacy Scale

时间窗: Score at baseline and 6 weeks

Validated measure of self-efficacy. Minimum 0 - Maximum 60; higher score means a better outcome

次要结局

  • Change in Interstitial Cystitis Problem Index(Scores at baseline and 6 weeks)
  • Change in Hospital Anxiety and Depression Scale - Anxiety Subscale(Score at baseline and 6 weeks)
  • Change in Interstitial Cystitis Symptom Index(Score at baseline and 6 weeks)
  • Change in Hospital Anxiety and Depression Scale - Depression Subscale(Score at baseline and 6 weeks.)
  • Change in Brief Health Care Climate Questionnaire(Score at baseline and 6 weeks)

研究者

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

Lily Arya

Chief, Urogynecology and Reconstructive Surgery

University of Pennsylvania

研究点 (1)

Loading locations...

相似试验