Viewing Study NCT06145997



Ignite Creation Date: 2024-05-06 @ 7:49 PM
Last Modification Date: 2024-10-26 @ 3:14 PM
Study NCT ID: NCT06145997
Status: NOT_YET_RECRUITING
Last Update Posted: 2023-12-15
First Post: 2023-11-12

Brief Title: Feasibility and Acceptability Study of ACUAWARE
Sponsor: University of Utah
Organization: University of Utah

Study Overview

Official Title: Collecting Pragmatic Data Via Electronic Health Records ACUAWARE Feasibility and Acceptability Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2023-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ACUAWARE
Brief Summary: This study aims to gather preliminary feasibility and acceptability data to justify a subsequent trial that would fill a gap in knowledge regarding acupuncture therapy AT effects on interoceptive awareness IA among those with chronic pain
Detailed Description: This study aims to gather preliminary feasibility and acceptability data to justify a subsequent trial that would fill a gap in knowledge regarding acupunctures effects on interoceptive awareness among individuals with chronic pain Our primary hypotheses are that 1 Feasibility it is feasible for us to enroll and retain 70 of the patients and it is feasible to collect data from at least 70 of participants at 3-months follow-up and 2 Acceptability it is acceptable for 70 of licensed acupuncturists to use Acu-Track Registry it is acceptable for 70 of patients to complete questionnaires emailed to them via Acu-Track Registry

The investigators propose to evaluate these hypotheses by conducting a prospective pragmatic single-arm feasibility and acceptability study among individuals with chronic pain of any etiology or location except if due to cancer Chronic pain is defined as pain that persists or recurs for more than 3 months

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None