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Assessment of a combined manual therapy and taping method for the treatment of chronic lower back pain: A randomized controlled trial

Assessment of a combined manual therapy and taping method for the treatment of chronic lower back pain: A randomized controlled trial - MEDI-TAPING

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
DRKS
Registry ID
DRKS00017051
Enrollment
100
Registered
2019-07-24
Start date
2015-06-09
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

CHRONIC LOWER BACK PAIN

Interventions

Group 1: Medi-Taping: received three treatments within three weeks on average Group 2: Standard Treatment: received booklet containing psychoeducative information for patients with lower back pain and

Sponsors

Dept. for Psychosomatic Medicine and Psychotherapy, Medical Faculty, Medical Center – University of Freiburg, Germany
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: unspecific lower back pain for more than 12 weeks, a rating of at least 4 cm on a 10 cm Visual Analog Scale (VAS) for the back pain, the ability to read and communicate in German

Exclusion criteria

Exclusion criteria: neurological malfunction at the lower extremities related to CLBP, a rating larger than 8cm on the VAS for back pain, back pain due to infection, tumor, osteoporosis, stenosis of the cerebrospinal canal, slipped vertebra, vertebral fractures, spinal disc herniation, surgery of vertebra, spinal disc or sacroiliac joint. Furthermore allergy to tape, pregnancy, current cancer diagnosis, addictive disorder, severe psychiatric disorder, significant impairment due to memory problems or brain disorders, artificial hip ankle or knee joint, participations in other RCTs

Design outcomes

Primary

MeasureTime frame
changes at t2 for pain (VAS and Korff pain grade), and functional limitations (Oswestry Disability Score)

Secondary

MeasureTime frame
changes in quality of life (PLC), spinal mobility (Schober Sign Test and Distance Fingertips to Floor) and leg length difference (as indicator of pelvic obliquity) at t2 and all changes at t3

Countries

Germany

Contacts

Public ContactStefan Schmidt

Klinik für Psychosomatische Medizin Universitätsklinikum Freiburg

stefan.schmidt@uniklinik-freiburg.de+49-761-270-69280

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 23, 2026