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Web-Based Exercise Program for Non-Specific Low Back Pain (WEBEX-LBP)

M

Medipol University

Status

Not yet enrolling

Conditions

Non-specific Low Back Pain (NSLBP)

Treatments

Behavioral: Web-Based Therapeutic Exercise Program
Behavioral: Traditional Home Exercise Program

Study type

Interventional

Funder types

Other

Identifiers

NCT07208435
E-10840098-202.3.02-3388

Details and patient eligibility

About

This study evaluates the effectiveness of a web application-based exercise program (delivered via Physitrack) for managing non-specific low back pain (NSLBP) compared to traditional home exercise programs. The trial focuses on whether web-based delivery can improve pain, function, quality of life, and adherence, providing evidence for digital rehabilitation as a practical alternative to conventional physiotherapy.

Full description

Non-specific low back pain (NSLBP) is a prevalent condition associated with pain, functional limitations, and reduced quality of life. Access to in-person physiotherapy can be limited by geographic, financial, or time-related constraints. Web-based exercise programs offer an accessible alternative by delivering personalized exercises, educational content, reminders, and self-monitoring tools via digital platforms.

This study aims to investigate whether a structured web application-based exercise program can improve outcomes for adults with NSLBP compared to traditional home exercises. The trial addresses gaps in current evidence regarding the effectiveness of telerehabilitation, patient engagement, and delivery modes, and seeks to determine if digital interventions can serve as a viable complement or alternative to conventional physiotherapy.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults aged 18-45 years diagnosed with non-specific low back pain (NSLBP) for 6 weeks to <12 months.
  • Self-reported pain intensity ≥3 on a 0-10 Numeric Pain Rating Scale (NPRS).
  • Evidence of functional limitation (Oswestry Disability Index or Roland-Morris Disability Questionnaire).
  • Access to a smartphone, tablet, or computer with internet connectivity.
  • Ability and willingness to participate in telerehabilitation programs.

Exclusion criteria

  • Specific causes of low back pain (herniated disc with radiculopathy, spinal stenosis, spondylolisthesis, fractures, infections, malignancy).
  • Neurological deficits (e.g., severe motor weakness, progressive neurological symptoms).
  • Severe psychiatric or cognitive disorders interfering with participation.
  • History of spinal surgery within the last year.
  • Severe comorbidities contraindicating exercise (e.g., uncontrolled diabetes, cardiovascular disease).
  • Pregnant or planning pregnancy during the study period.
  • Active substance or alcohol abuse.
  • Participation in other structured rehabilitation or physical therapy programs within the last 3 months.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Web-Based Exercise Program
Experimental group
Description:
Participants complete an 8-week web-based exercise program via Physitrack. Sessions last 30-45 minutes, twice per week, focusing on core strengthening, spinal mobility, posture correction, and pain reduction. Exercises progress weekly from basic core engagement to advanced trunk control and integration.
Treatment:
Behavioral: Web-Based Therapeutic Exercise Program
Traditional Home Exercise Program
Active Comparator group
Description:
Participants complete a 6-week traditional home exercise program. Sessions last 30-40 minutes, focusing on flexibility, basic trunk and core strengthening, balance, and ergonomic practice. Exercises progress weekly, emphasizing pain relief, trunk mobility, and functional strength.
Treatment:
Behavioral: Traditional Home Exercise Program

Trial contacts and locations

1

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Central trial contact

Yağmur Mustafaoğlu, PT, MSc (Cand.)

Data sourced from clinicaltrials.gov

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