Effects of Mulligan SNAG in Chronic Nonspecific Low Back Pain
CompletedNot applicableNCT07415538
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The aim of this randomized controlled study was to compare the effects of Mulligan SNAG added to conventional physiotherapy with conventional physiotherapy alone and sham SNAG on pain, function, proprioception, and functional performance in individuals with chronic nonspecific low back pain.
Study details
- Official title
- Effects of Mulligan SNAG Compared With Conventional and Sham Therapy in Chronic Nonspecific Low Back Pain
- Conditions
- Nonspecific Chronic Low Back Pain
- Pain
- Manuel Therapy
- Physical Therapy
- Interventions
- Other: Conventional Physiotherap
- Other: Conventional Physiotherapy + Mulligan SNAG
- Other: Conventional Physiotherapy + Sham SNAG
- Sponsor
- Biruni University
- Start date
- 2026-01-05
- Primary completion
- 2026-02-13
- Sex
- All
- Age range
- from 18 Years to 65 Years
- Results posted
- No results posted in this snapshot
- Countries
- Turkey (Türkiye)
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Adults aged between 18 and 65 years * Presence of chronic nonspecific low back pain lasting for at least 6 months * No signs or symptoms of radicular pain or progressive neurological deficit * No history of lumbar spine surgery * No manual therapy, spinal injection, or structured physiotherapy program for low back pain within the last 3 months * Ability to participate in a physiotherapy and exercise program * Willingness to participate in the study and provision of written informed consent Exclusion Criteria: * Specific causes of low back pain (e.g., fracture, tumor, infection, inflammatory spinal disorders) * Presence of radiculopathy or severe neurological impairment * History of spinal surgery * Pregnancy * Severe balance, vestibular, or neurological disorders that may interfere with proprioception testing * Any medical condition contraindicating physical therapy or manual therapy * Participation in another clinical trial or receiving concurrent treatment for low back pain during the intervention period
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07415538