Skip to content

Effect of Video-based Stabilization Exercises on Pain, Function, Adherence, Kinesiophobia & QoL in NSCBP Patients

The Effects of Video-Based Stabilization Exercises on Pain, Functionality, Exercise Adherence, Kinesiophobia, and Qol in Individuals With NSCBP

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07005765
Enrollment
42
Registered
2025-06-05
Start date
2025-03-03
Completion date
2025-04-14
Last updated
2025-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise Therapy, Non Specific Chronic Low Back Pain

Keywords

Chronic Low Back Pain, Core Exercise, Exercise Adherence

Brief summary

This randomized controlled study aims to evaluate the effectiveness of a 6-week home-based stabilization exercise program in individuals with non-specific chronic low back pain. Participants will be randomly assigned to two groups: one receiving exercise instruction via video-based content, and the other via a printed brochure with illustrated exercises. The effectiveness of the interventions will be assessed in terms of pain severity, functional status, exercise adherence, kinesiophobia, and quality of life.

Detailed description

This study investigates the effectiveness of a 6-week home-based core stabilization exercise program in individuals with non-specific chronic low back pain (NSCLBP). The purpose is to compare two different delivery methods of the same exercise protocol: video-based versus illustrated brochure-based instructions. Stabilization exercises are commonly used in NSCLBP management; however, the mode of delivery in home settings can impact adherence and clinical outcomes. A total of 42 participants with NSCLBP will be randomly assigned to either the video-based group or the brochure-based group. Both groups will follow the same exercise content, frequency, and duration. Outcomes will be assessed at baseline and after 6 weeks using standardized tools for pain (Visual Analog Scale), functional status ( Oswestry Disability Index), exercise adherence (Exercise Adherence Rating Scale), kinesiophobia (Tampa Scale), and quality of life (SF-36). The findings will be contribute to the optimization of home exercise strategies for chronic low back pain management.

Interventions

BEHAVIORALVideo-Based Stabilization Exercise Program

Participants will follow a 6-week home exercise program focusing on stabilization exercises. The instructions and demonstrations will be delivered through video format, which participants can watch at their convenience. The program aims to improve pain, functionality, exercise adherence, kinesiophobia, and quality of life.

BEHAVIORALBrochure-Based Stabilization Exercise Program

Participants will follow the same 6-week home exercise program using illustrated printed brochures that provide step-by-step instructions for stabilization exercises. This format allows participants to perform exercises independently. The program's effects on pain, functionality, exercise adherence, kinesiophobia, and quality of life will be evaluated.

Sponsors

Serra Sürel
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Participants will be blinded to their group assignment and will not know whether they receive video-based or brochure-based exercise instructions. However, investigators delivering the interventions will be aware of the assignments.

Intervention model description

Participants with non-specific chronic low back pain will be randomly assigned into two parallel groups. One group will receive a 6-week home-based stabilization exercise program delivered via video instructions, while the other group will receive the same exercise program using illustrated printed brochures. Both groups will follow the intervention independently without crossover. The effectiveness of the interventions will be compared between groups after 6 weeks.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Clinical diagnosis of non-specific chronic low back pain lasting 3 months or more Age 18 years or older Score of 4 or higher on the Roland-Morris Disability Questionnaire Voluntary agreement to participate in the study

Exclusion criteria

Physiotherapy treatment for low back pain within the past 6 months Pain radiating to the lower extremities Pregnancy History of spinal surgery Presence of central or peripheral nervous system pathology (e.g., stroke)

Design outcomes

Primary

MeasureTime frameDescription
KinesiophobiaBaseline and after 6 weeks of interventionKinesiophobia will be assessed using the Tampa Scale for Kinesiophobia (TSK), a validated self-report questionnaire that evaluates fear of movement or re-injury. The scale consists of 17 items rated on a 4-point Likert scale. The total score varies between 17 and 68. Higher scores indicate greater levels of fear.

Secondary

MeasureTime frameDescription
Pain IntensityBaseline and after 6 weeksPain will be measured using the Visual Analog Scale (VAS), scored from 0 (no pain) to 10 (worst pain).
Functional DisabilityBaseline and after 6 weeksFunctional disability will be assessed using the Oswestry Disability Index (ODI). The lowest score is 0 and the highest score is 50. Higher scores reflect greater disability.
Change in Quality of LifeBaseline and after 6 weeksQuality of life will be assessed with the Short Form-36 (SF-36), which evaluates physical, emotional, and social well-being. The total score varies between 0 (lowest quality of life score) and 100 (highest quality of life score).
Exercise AdherenceAt the end of the 6-week interventionExercise adherence will be assessed through an Exercise Adherence Rating Scale (EARS). Scoring ranges from 0 to 64. Higher scores indicate greater compliance with exercise.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026