Viewing Study NCT06546956



Ignite Creation Date: 2024-10-26 @ 3:37 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06546956
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-07-30

Brief Title: Integrative Breathwork Intervention for Chronic Pain
Sponsor: None
Organization: None

Study Overview

Official Title: Developing and Testing a Multicomponent Breathwork Intervention for Adults With Chronic Pain
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The proposed research is to develop and refine a multicomponent breathwork intervention Guided Respiration Mindfulness Therapy and to iteratively evaluate its feasibility acceptability and plausibility for clinically significant effects in people with chronic low back pain This integrative breathwork intervention involves a 60-minute breathing session where the focus is to maintain a conscious connected breathing pattern no pause between inhale and exhale apply mindful acceptance to somatic sensations and relax any physical tension Each breathwork session will be delivered 1-on-1 in person by a trained facilitator The treatment consists of 8 breathwork sessions once per week for 8 weeks
Detailed Description: Multiple single-arm iterations of an 8-week breathwork intervention will be conducted to refine and optimize the intervention and protocol Upon completion of each iteration quantitative and qualitative data will be gathered to identify possible modifications before proceeding with the next iteration This work will provide initial evidence on the feasibility acceptability and plausibility of clinically significant effects of this type of multicomponent breathwork intervention for adults with chronic low back pain

Study Oversight

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