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Completed

NCT Number: NCT00450606

The Effects of Ambulatory Treatment at the Dead Sea on Osteoarthritis of the Knees

This study will check the efficacy of balneological therapy of bathing in Dead Sea fountain waters over a 6 week period on a twice a week basis (overall 12 treatments) in patients suffering from osteoarthritis of the knees.

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Key information

Conditions

Osteoarthritis of the Knees

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Since stay in the Dead Sea for a long period of time is an expensive matter, it is important to determine whether twice a week treatments can be as beneficiary as two straight weeks of treatments as was shown to be effective in previous studies.

Our study will follow the patients for a longer period of time (6 months) than was done in previous studies.

An additional advantage will be separating the therapeutical effect of our specific treatment from the therapeutical effect of being in a comfortable hotel away from the daily nuisances for 2 weeks which by itself has been shown to be pain relieving in patients suffering from rheumatic diseases.

Our study will take 50 patients suffering from Osteoarthritis of the knees and divide them in to 2 equal groups. One group will be treated twice a week with thermo-mineral baths at the temperature of 35-36 degrees Celsius for approximately 20 minutes. The other group will be treated twice a week with hot sweet water tub (without the water jets!) of the same temperature and for the same length of time.

Both groups will change nothing in their current medical treatment.

The patients will be examined at 5 points during this study: a few days before their first treatment, right after their last treatment (after 6 weeks), after one month, after 3 months and after 6 months.

All examination will be performed in the Soroka University Medical Center.

The clinical indexes and questionnaires which would be filled during this trial will be:

  • WOMAC index
  • Lequesne's index
  • Visual analogue scale by the patient
  • Visual analogue scale by the doctor
  • SF 36 and Health assessment questionnaire (HAQ)

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients suffering from Osteoarthritis of the knees according to the conventional measurements of the American College of Rheumatology and who are treated in the Rheumatological clinics of the Soroka University Medical Center

Exclusion criteria

  • Patients suffering from any other rheumatological disease other than osteoarthritis
  • Patients that were previously treated with hydrotherapy or balneotherapy
  • Patients suffering from balance disorders or loss of consciousness disorders such as epilepsy, arrhythmias etc.

Treatment and study plan

Balneotherapy and hydrotherapy

Procedure

Primary outcomes

  1. Quality of life evaluation at one, three and six months

  2. Functional state of the patient at one, three and six months

  3. Osteoarthritis severity at one, three and six months

Sponsors and collaborators

Lead sponsor

Soroka University Medical Center

Other

Collaborators

  • Lot Spa Hotel Dead Sea

Registry information

Important dates

Study start
2007
Primary completion
2007
First posted
Mar 22, 2007
Registry last updated
May 21, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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