Effects of a CSE With ADIM in Chronic Non-specific Low Back Pain With Lumbar Instability Using Telerehabilitation.
CompletedNot applicableNCT06321393
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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 goal of this clinical trial is to compare the effectiveness of telerehabilitation-based and clinic-based methods to deliver a Core Stabilization Exercise Program with the Abdominal Drawing-In Maneuver Technique (CSE with ADIM) on pain intensity, functional ability, quality of life, and satisfaction in chronic low back pain patients with lumbar instability. The main question it aims to answer is: Is there a difference between the effectiveness of telerehabilitation-based and clinic-based CSE with ADIM on pain intensity, functional ability, quality of life, and satisfaction in chronic low back pain patients with lumbar instability? Participants will perform a 7-week core stabilization exercise with the abdominal drawing-in maneuver technique, consisting of an exercise program for 20-minute sessions with 3 sessions per week. These exercise programs will be provided to the participants via a weekly video call with the main researcher as a telerehabilitation program. At the first session of each week, the researcher will provide supervision via video call with the participant for the exercise program. The participants will perform the exercise by following the video demonstration. After completing weekly training, participants will perform their exercise routine as part of their daily home program. If there is a comparison group: researchers will compare The control group (clinical-base group) will be provided the 7-week core stabilization exercise with abdominal drawing-in maneuver technique, the same as the experimental group, but control groups received the exercise program at the clinic according to the usual methods. At the first session of each week, an appointment will be set, and then the specific exercise for each week will be delivered and trained by the main researcher at the clinic. After completing weekly training, participants will perform their exercise routine as part of their daily home program to see if there are any differences in pain intensity, f…
Study details
- Official title
- Effects of a Core Stabilization Exercise Program With the Abdominal drawing-in Maneuver Technique in Chronic Non-specific Low Back Pain With Lumbar Instability Using Telerehabilitation.
- Conditions
- Chronic Low-back Pain
- Lumbar Instability
- Interventions
- Other: 7-week Core stabilization exercise with abdominal drawing-in maneuver technique
- Sponsor
- Khon Kaen University
- Start date
- 2024-02-01
- Primary completion
- 2025-04-09
- Sex
- All
- Age range
- from 18 Years to 60 Years
- Results posted
- No results posted in this snapshot
- Countries
- Thailand
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Males or females. 2. Aged between 18 - 60 years old. 3. Onset of back pain lasting more than 12 weeks. 4. Lumbar instability will be diagnosed using a score of at least 6 out of 14 on the Screening Tool for Patients with Lumbar Instability Questionnaire in Thai version. 5. Presented at least two positive signs from three special tests of the following provocation tests: Painful catch, aberrant movement sign, or prone instability test. 6. Pain intensity at rest has a pain level with a numerical rating scale (0-10 NRS) 3-7/10 points. 7. Never receive the treatment by core stabilization exercise during 3 months before participate in this study. 8. Participants must have a smart phone, tablet, or other electronic device with a camera and install the line application on the device. They can perform the basic operations of these devices by themselves. 9. Participants have the ability to read and write Thai fluently. Exclusion Criteria: 1. Onset of serious spinal pathology: spinal fracture, spinal malignancy, or spinal infection. 2. Have been diagnosed with osteoporosis, ankylosing spondylitis, or spondyloarthritis. 3. History of spinal surgery and/or lower extremity. 4. Cauda equina syndrome. 5. Presented at least 2 out of 3 signs of neurological deficit including reflex abnormality or loss of sensation of lower limbs associated with the spinal nerve root and weakness of lower limbs (muscle power less than grade 3 using manual muscle test) (Macedo et al., 2008). 6. Pregnancy or during breast feeding. 7. Body mass index (BMI) \> 30 kg/m2.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06321393