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Randomized controlled single-blind study in a repeated-measurement design to compare the effects of serial mud- and heat packs on functional health parameters in patients with degenerative diseases of the spine.

Randomized controlled single-blind study in a repeated-measurement design to compare the effects of serial mud- and heat packs on functional health parameters in patients with degenerative diseases of the spine.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00031893
Enrollment
112
Registered
2023-05-16
Start date
2023-08-15
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

Presence of a radiologically confirmed thoracic and/or lumbar osteochondrosis (ICD-10-GM: M42.1-, M42.9-) (excluding patients with isolated affected occipito-atlanto-axial area and cervical area).

Interventions

Group 1: The patients from group I receive 6 serial treatments with mud packs within 21 days (2x per week, 20 minutes each). Group 2: The patients from group II receive 6 serial treatments with heat p

Sponsors

KURPARK KLINIK Bad Nauheim
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Age 18-70y; Radiologically confirmed lumbar and/or thoracic osteochondrosis and/or chronic thoracic Backpain (M42.1-, M42.9-); Barthel-Index >70

Exclusion criteria

Exclusion criteria: Age 70y; bodyweight >150kg, radikulopathies, wounds in the area of treatment; Red flags of the spine; known allergies; Previous operations on the spine; local glucocorticoid injection 1 non-appearance for therapy or Rehab-cancellation; Rheumatic disease

Design outcomes

Primary

MeasureTime frame
Oswestry Disability Index ODI-G Version 2.1b Data collection times: Pre- and post-interventional (after 3 weeks) as well as in a 6-week postal follow-up after the last intervention.

Secondary

MeasureTime frame
CRP i.S. and leukocyte count, FFD (finger floor distance) SF12, FABQ (German fear avoidance belief questionnaire), NRS, Pain Medication & Dosage Data collection times: Pre- and post-interventional (after 3 weeks) as well as in a 6-week postal follow-up after the last intervention.

Countries

Germany

Contacts

Public ContactMartin Oswald

Justus Liebig Universität Gießen

Martin.S.Oswald@med.uni-giessen.de+4915233677624

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026