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Effectiveness of an osteopathic Treatment in Patients suffers from Achilles Tendinopathy. A randomized controlled trial

Effectiveness of an osteopathic Treatment in Patients suffers from Achilles Tendinopathy. A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00014975
Enrollment
100
Registered
2018-09-04
Start date
2014-09-01
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

M76.6

Interventions

Group 1: Eight treatment sessions within a time period of four weeks with manipulation techniques (HVLA) + a fascial treatment of the upper limb. Group 2: Home based eccentric muscle training for th

Sponsors

stillpoint-Praxis für Osteopathie und Naturheilkund
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) aged between 35 to 60 years; (2) Achilles tendon pain at least one on a visual analogue scale (VAS); (3) pain duration > 12 weeks

Exclusion criteria

Exclusion criteria: (1) if they suffered from systemic conditions, such as diabetic, heart disease, metabolic disease; (2) severe orthopaedic disorder; (3) any kind of treatment of the Achilles tendon during the last two weeks; (4) any kind of surgery on the Achilles tendon; (5) Achilles tendon rupture in the past; (6) or pregnancy.

Design outcomes

Primary

MeasureTime frame
self-reported pain intensity, measured by the Visual analogue scale (VAS) before and after the treatment. Severity of Achilles tendinopathy, measured by the VISA-A questionnaire, before and after the treatment.

Secondary

MeasureTime frame
Postural stability measured by the BESS test before and after the treatment. Range of motion (ROM) of the upper ankle Joint before and after the treatment.

Countries

Germany

Contacts

Public ContactKatrin Brück

stillpoint-Praxis für Osteopathie und Naturheilkund

info@still-point-geestland.de0049 4742 3442606

Outcome results

None listed

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