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Patient Adherence to Acupuncture Treatment

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ClinicalTrials.gov Identifier: NCT03645083
Recruitment Status : Completed
First Posted : August 24, 2018
Last Update Posted : August 24, 2018
Sponsor:
Information provided by (Responsible Party):
David Black, University of Southern California

August 22, 2018
August 24, 2018
August 24, 2018
February 20, 2017
August 24, 2017   (Final data collection date for primary outcome measure)
Attendance to follow-up treatment [ Time Frame: Within 30 days after participants' initial visit ]
Participants attending acupuncture follow-up treatments
Same as current
No Changes Posted
Total number of follow-up treatments [ Time Frame: Within 30 days after participants' initial visit ]
The total number of follow-up treatments by participants
Same as current
Not Provided
Not Provided
 
Patient Adherence to Acupuncture Treatment
Improving Treatment Adherence in Acupuncture Patients: A Randomized Controlled Trail
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.

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.

Number of follow-up treatments for the same health concern will be collected for all enrolled participants from the participants' clinical record.

Interventional
Not Applicable
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description:
Randomized controlled trial
Masking: None (Open Label)
Primary Purpose: Health Services Research
Adherence, Patient
  • Behavioral: Telephone call
    Participants in the intervention group receive a one-time telephone call reminder to attend follow-up treatment at the acupuncture clinic
  • Behavioral: Text message
    Participants in the intervention group receive a one-time text messaging reminder to attend follow-up treatment at the acupuncture clinic
  • Experimental: Telephone call
    Participants receive a telephone call reminder three days after their initial visit
    Intervention: Behavioral: Telephone call
  • Experimental: Text message
    Participants receive a text message reminder three days after their initial visit
    Intervention: Behavioral: Text message
  • No Intervention: Control
    Participants do not receive any intervention after their initial visit
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
121
Same as current
October 31, 2017
August 24, 2017   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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
Sexes Eligible for Study: All
18 Years and older   (Adult, Older Adult)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT03645083
HS-17-00008
No
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Plan to Share IPD: No
Plan Description: No plan to share IPD
David Black, University of Southern California
University of Southern California
Not Provided
Study Director: David Black, PhD University of Southern California
University of Southern California
August 2018

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP