An Innovative and Linguistically-Tailored Mobile Intervention to Improve Follow-Up for Abnormal Pap Test Results: CervixChat
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Patient Consent Rate
研究概览
简要总结
This clinical trial evaluates the feasibility of a linguistically-tailored mobile intervention, called CervixChat in improving the follow-up of patients with abnormal Papanicolaou (pap) test results. A text messaging program, such as CervixChat may support patients who need a colposcopy.
详细描述
PRIMARY OBJECTIVE:
I. To evaluate the feasibility of CervixChat intervention in a mix method design, through participants consent rate and the study completion rate.
SECONDARY OBJECTIVE:
I. To evaluate the acceptability of CervixChat intervention using a validated Likert-scale participant satisfaction questionnaire, as well as participant's interview data.
EXPLORATORY OBJECTIVE:
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 21 Years 至 65 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Female, aged 21 to 65 years of age
- •Had received an abnormal Pap smear result
- •Scheduled colposcopy
- •Able to communicate with ease in English or Spanish
- •Have a cell phone with text (TXT) ability
- •Competent to give consent
排除标准
- •Are pregnant at the time of recruitment
- •Display current evidence of positive invasive carcinoma of the cervix
研究组 & 干预措施
Supportive care (message)
Patients receive text messages for 1-2 months before scheduled appointment. Patients also complete a survey at baseline and after standard of care colposcopy and an interview after standard of care colposcopy.
干预措施: Health Promotion and Education (Other)
Supportive care (message)
Patients receive text messages for 1-2 months before scheduled appointment. Patients also complete a survey at baseline and after standard of care colposcopy and an interview after standard of care colposcopy.
干预措施: Survey Administration (Other)
Supportive care (message)
Patients receive text messages for 1-2 months before scheduled appointment. Patients also complete a survey at baseline and after standard of care colposcopy and an interview after standard of care colposcopy.
干预措施: Interview (Other)
结局指标
主要结局
Patient Consent Rate
时间窗: Up to 12 months
Study Completion Rate
时间窗: Up to 12 months
次要结局
未报告次要终点