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Effects of Foundation and Functional Inspiratory Muscle Training in Non-Specific Chronic Low Back Pain

StatusRecruiting
PhaseNot applicable
Started2024-12-15
View on ClinicalTrials.gov ↗
Record status
This record was last updated December 31, 2024 (before its estimated July 1, 2026 completion). Its status may not reflect the trial's current state.

Amendment history

2024-12-29
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v2
Trial statusNot Yet Recruiting→Recruiting
Start dateestimated 2024-12-01→confirmed 2024-12-15
Study sitesdetails revised at 1 of 1 site
2024-11-29
minor
Study Status, Outcome Measures v1
Secondary endpointsdetails revised at 1 of 12 entries
2024-11-18
minor
Original filing
This study was planned to examine the effects of basic and functional respiratory muscle training on pain, disability level, and functionality. In this study, participants will be randomly divided into 3 groups. The first group will be treated with physical therapy applications applied in state hospitals for 10 weeks. The second group will receive basic respiratory muscle training treatment in addition to physical therapy in state hospitals. The third group will receive respiratory muscle training with exercise in addition to physical therapy in state hospitals. Evaluations will be made before the first session, after the 30th session, in the 3rd month, in the 6th month, and in the 1st year. There is no interventional method in the evaluations. Pain intensity, disability level, physical activity status, quality of life, fear of movement, pain catastrophizing, anxiety and depression levels will be questioned with scales. In physical measurements, participant's aerobic capacity will be measured with the 2-Minute Walk Test, participants's flexibility with the sit-and-long test, participants's respiratory muscle strength with the MIP/MEP device, participants's core endurance with the trunk flexor muscle endurance test, participants's lower and upper extremity muscle strength with a handheld dynamometer, participants's postural control with the Biodex balance device, and participants's muscle thickness with an ultrasound.
Trial Details
NCT Number NCT06696300
Lead Sponsor Kirsehir Ahi Evran Universitesi
Collaborators: Hacettepe University, Selcuk University
Conditions Low Back Pain, Mechanical, Low Back Pain, Chronic, Non Specific Chronic Low Back Pain
Enrollment 60 participants
Start Date 2024-12-15
Primary Completion 2026-07-01 (estimated)
Study Completion 2026-12-01 (estimated)
Updated on ClinicalTrials.gov 2024-12-31