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临床试验/NCT03645083
NCT03645083已完成不适用

Improving Treatment Adherence in Acupuncture Patients: A Randomized Controlled Trail

University of Southern California1 个研究点 分布在 1 个国家目标入组 121 人开始时间: 2017年2月20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
121
试验地点
1
主要终点
Attendance to follow-up treatment

研究概览

简要总结

Adherence to treatment recommendation remains low among acupuncture patients. This study aims to examine whether implementing a post-initial visit follow-up strategy can improve adherence rate. Adult patients visiting the acupuncture clinic for a new treatment will be randomized to receive a telephone call or a text-message three days after their initial visit against a control group. We will enroll up to 160 participants between February and December 2017, to ensure we can reach 120 subjects in the analysis who completed the baseline survey. Participants recruitment will take place at the Emperor's College of Traditional Oriental Medicine Acupuncture Clinic. Assessments will be conducted via surveys at four times points, Day 0 (date of enrollment), Day 3, Day 10 and Day 30. Additional data will also be collected via chart review. Primary outcome will be assessing whether participants return for any follow-up visit within 30 days after the initial treatment. Secondary outcomes will examine if factors such as expectations, intention, satisfaction, and potential barriers would predict the primary outcome.

详细描述

This randomized controlled trial will deliver two interventions: (1) telephone call reminder and (2) text messaging reminder.

Participants who meet study eligibility criteria based on intake assessment will be recruited and complete baseline assessment immediately after they receive acupuncture treatment. There will be 40 participants in each of the two intervention groups and the no intervention control group.

Participants will be adults who visit the Emperor's College Acupuncture Clinic for a new treatment consultation on the date of the enrollment.

The telephone call and text messaging intervention is a one-time reminder system delivered to the participants based on the study random assignment, three days after the initial visit. A research assistant will be contacting the participants based on the assigned interventions.

There are three data collection points, 1) baseline (during initial visit), 2) 10 days after the initial visit, and 3) 30 days after the initial visit. Data will be collected via a tablet (baseline) and online survey (Day 10 and Day 30) through a secure online survey platform. Baseline assessment will occur prior to randomization, and post-intervention assessments will occur at 10 to 30 days after the initial visit.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Outside patients seeking acupuncture treatment at Emperor's College Clinic
  • •Age 18 and above
  • •English-speaking
  • •Starting a new treatment at the day of recruitment
  • •Own a mobile device
  • •Mobile device has text-messaging capability
  • •Visiting the Master's Clinic at Emperor's College

排除标准

  • •Emperor's College's students or staffs seeking acupuncture treatment
  • •Patients visiting the faculty observation theater, ear acupuncture clinic and private clinic
  • •Patients returning for a follow-up acupuncture visit at the day of recruitment

研究组 & 干预措施

Telephone call

Experimental

Participants receive a telephone call reminder three days after their initial visit

干预措施: Telephone call (Behavioral)

Text message

Experimental

Participants receive a text message reminder three days after their initial visit

干预措施: Text message (Behavioral)

Control

No Intervention

Participants do not receive any intervention after their initial visit

结局指标

主要结局

Attendance to follow-up treatment

时间窗: Within 30 days after participants' initial visit

Participants attending acupuncture follow-up treatments

次要结局

  • Total number of follow-up treatments(Within 30 days after participants' initial visit)

研究者

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

David Black

Assistant Professor of Preventive Medicine

University of Southern California

研究点 (1)

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