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Effects Of GDS Method Along With CBTThrough Smartphone Health App For Patients With Chronic LDP

Effects Of Godelieve Denis-Struf (GDS) Method Along With Cognitive Behavioral Therapy Through Smartphone Health App For Patients With Chronic Lumbosacral Discogenic Pain.

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07068321
Enrollment
159
Registered
2025-07-16
Start date
2025-04-17
Completion date
2026-06-01
Last updated
2025-07-16

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

Conditions

Lumbosacral Disc Syndrome

Brief summary

Chronic lumbosacral discogenic pain is a common and debilitating condition that significantly affects the quality of life of patients. Traditional treatments often focus on pain management, but a holistic approach combining physical exercises and psychological therapy can offer more sustainable relief.

Detailed description

The Godelieve Denis-Struf (GDS) method has been shown to improve posture, mobility, and muscular imbalances in patients with musculoskeletal pain. Cognitive Behavioral Therapy (CBT) is another effective intervention that addresses the psychological factors contributing to chronic pain. With the rise of digital health solutions, smartphone applications have emerged as convenient tools to deliver these therapeutic methods. This study explores the combined effects of GDS exercises and CBT via a smartphone health app for individuals suffering from chronic lumbosacral discogenic pain.

Interventions

COMBINATION_PRODUCTControl Group (transcutaneous electrical nerve stimulation)

Control Group will consist of 20 sessions of 30 min, applied twice per week over a period of 3 months including transcutaneous electrical nerve stimulation, and standardized exercises for LBP through smart phone application.

COMBINATION_PRODUCTGodelieve Denis-Struf

Experimental Group will receive 20 sessions of 30 min applied twice per week over a period of 3 months of GDS treatment through smart phone application.

COMBINATION_PRODUCTGodelieve Denis-Struf + Cognitive Behavioral Therapy

Experimental Group 2 will receive 20 sessions of 45 min applied twice per week over a period of 3 months of GDS along CBT treatment through smart phone application.

Sponsors

Superior University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

* Age of 40 to 65 years * Diagnosed chronic lumbosacral discogenic pain by a physician or neuro-physician. * No surgical history of lumbosacral area

Exclusion criteria

* Pregnancy * Diagnosis of cancer * Fibromyalgia or inflammatory disease (eg, rheumatoid arthritis or spondylitis) * Surgical cases of lumbosacral area * comorbidity like uncontrolled diabetes and blood pressure

Design outcomes

Primary

MeasureTime frameDescription
The Oswestry Disability Index (ODI)18 MonthsThe Oswestry Disability Index (ODI) is a questionnaire used to assess the impact of low back pain on a person's daily life. It consists of 10 sections, each with six statements, and patients select the statement that best describes their situation. Each section is scored from 0 to 5, with 0 indicating no disability and 5 indicating the worst imaginable disability. The total score is then calculated and can be expressed as a percentage, with a higher score indicating greater disability
SF-36 (Short Form 36)18 MonthsThe SF-36 (Short Form 36) is a questionnaire used to assess health-related quality of life, encompassing both physical and mental well-being. It consists of 36 items that evaluate eight health domains: physical functioning, role limitations due to physical health, bodily pain, general health perceptions, vitality, social functioning, role limitations due to emotional problems, and mental health. Scores for each domain range from 0 to 100, with higher scores indicating better health

Countries

Pakistan

Outcome results

None listed

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