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Spa Rehabilitation After Cruciate Ligament Injury in Sportsmen

Comparison Between Two Rehabilitation Programs (Conventional and Aquatic) After Cruciate Ligament Injury in Sportsmen

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02225613
Acronym
Thermasport
Enrollment
128
Registered
2014-08-26
Start date
2014-10-31
Completion date
2017-10-31
Last updated
2016-08-08

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

Conditions

Balance Control, Cruciate Ligament Injury

Keywords

Cruciate ligament injury, Balance control, Rehabilitation, Spa therapy, Sport

Brief summary

Knee cruciate ligament injury is a common injury (15 000 per year in France) which concerns young sportsmen. Consequences are limitation in physical and sporting activities and at work. Main objective: to compare water and traditional rehabilitation after cruciate ligament injury reconstruction in terms of kinematics of recovery and of proprioceptive abilities development.

Detailed description

Secondary objectives: to compare algo-functional and sport, social and job come back date between both groups. Multicentric randomised trial comparing two therapy protocols in knee cruciate ligament injury. After surgery, 2 weeks rehabilitation; 3 weeks conventional rehabilitation (group 1) or rehabilitation in water (group 2). Data will be collected at inclusion (before surgery), 2 weeks, 1 month, 2 months and 6 months after surgery.

Interventions

OTHERUsual protocol
OTHERSpa protocol

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 49 Years
Healthy volunteers
No

Inclusion criteria

* Adults, * 18-49 years, * indication of knee anterior cruciate ligament reconstruction.

Exclusion criteria

* other recent lower limb sprain, * history of neurological disease (stroke, central or peripheral degenerative disease), * psychtrope or antihypertensive drugs, * aquatic activities contra-indication (cutaneous).

Design outcomes

Primary

MeasureTime frameDescription
Posturography composite scoreup to 6 monthsPostural control during quiet stance will be evaluated without and with sensory conflict by a sensory organization test

Countries

France

Contacts

Primary ContactPhilippe Perrin, MD, PhD
philippe.perrin@univ-lorraine.fr+333 83 15 49 68

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026