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Study on the evaluation of hippotherapy in the course of treatment for multiple sclerosis - a prospective, randomized controlled and multicenter study

Study on the evaluation of hippotherapy in the course of treatment for multiple sclerosis - a prospective, randomized controlled and multicenter study - MS-Hippo

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00005289
Enrollment
70
Registered
2013-10-09
Start date
2013-09-02
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

G35

Interventions

Group 1: intervention group: hippotherapy (12 weeks, once a week for 30 minutes) Group 2: control group (unchanged continuation of the physiotherapy according to the remedy guidelines
unchanged continuation of the pharmacotherapy)

Sponsors

Zentrum für Therapeutisches Reiten Johannisberg e.V.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Definite multiple sclerosis with spasticity of the lower limbs; EDSS-Score between 4 and 6.5; Presence of an informed consent form signed by the patient; Consent of the responsible investigator; Legal capacity; Minimum age of 18 years

Exclusion criteria

Exclusion criteria: Hippotherapy within the last 12 months; Parallel participation in other interventional studies; Persons, who have an employment relationship/ a relationship of dependency on the sponsor or the investigator Placing in an institution because of responsible governmental or judicial authorities; Body weight above 90 kg; Acute episode between 4 weeks prior to the start of the therapy; No balance while sitting; Planned start of an new spasmolytic drug or drugs, which could influence the tested parameters (for example Sativex®; Injection of Baclofen close to the spinal cord, 4-Aminopyridin); cerebral seizure disorder, that is not medically adjusted; No or insufficient ability to spread out the legs, which is necessary to sit on a horse; Heavy osteoporosis; Heavy arthrosis of the hip joint; Heavy scoliosis, which could deteriorate under hippotherapy; Heavy disorder of blood clotting, which increase the risk for bleedings because of hippotherapy Unstable internal, gynaecological, surgical secondary illness; Insurmountable fear of horses; Allergy against horsehair; Pregnancy

Design outcomes

Primary

MeasureTime frame
Change in balance ability: Change of Berg-Balance-Scale (BBS) after 12 weeks of hippotherapy (relative to the initial value)

Secondary

MeasureTime frame
Change in fatigue: Fatigue Severity Scale (FSS) after 12 weeks of hippotherapy (relative to the initial value); Change in quality of life: Multiple Sclerosis Quality of Life-54 (MSQOL-54) after 12 weeks of hippotherapy (relative to the initial value); Change in pain intensity: Visual Analogue Scale (VAS) after 12 weeks of hippotherapy (relative to the initial value); Change in spasticity: Numeric Rating-Scale (NRS) after 12 weeks of hippotherapy (relative to the initial value)

Countries

Germany

Contacts

Public ContactMarion Drache

Zentrum für Therapeutisches Reiten Johannisberg e.V.

md@johannisberg.net01722527037

Outcome results

None listed

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