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Whiplash Associated DisordersNCT00266981

Treatment of Whiplash Associated Disorders by APOS Kit

A study testing APOS - exercise component in people with Whiplash Associated Disorders and Cervical Pain, run by Hadassah Medical Organization at 1 site in Israel.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The purpose of this study is to compare two techniques for treating patients with Whiplash Associated Disorders, in relation to: disability, balance, cervical pain and cervical range of motion. The hypothesis: The APOS kit treatment is more effective than the short wave therapy. Read more about this study

Who is it for?
Ages 16 to 70 years
Conditions the study is for
Whiplash Associated Disorders, Cervical Pain
What is being tested?
APOS - exercise component
Type of treatment
Medical device
How many people
132 participants
Where
1 siteIsrael
Study dates
Mar 2006to Dec 2006
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 to 70 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Inclusion Criteria:Cervical pain, Motor vehicle accident a week prior to cervical pain, age above 16, ability to walk independently, signed inform consent, insured in "Clalit health services" Exclusion Criteria: Inability to walk independently, age 16 or less, not signed an inform consent, WAD grade 4, past treatment for WAD, pregnancy, pacemaker, cancer.

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Trial locations and contacts

1 site in 1 country.

Israel1 site
  • Hadassah Medical Organization

    Jerusalem

    Arik Tzukert, DMD, 00 972 2 6776095, arik@hadassah.org.il

    Hadas Lamberg, PhD, 00 972 2 6777572, lhadas@hadassah.org.il

Other trials in Israel

About this study

Official title: A Randomized Controlled Trial Which Compare the Effectiveness of an APOS Kit With Short Waves Therapy for Treating Whiplash Associated Disorders

The purpose of this study is to compare two techniques for treating patients with Whiplash Associated Disorders, in relation to: disability, balance, cervical pain and cervical range of motion.

The hypothesis: The APOS kit treatment is more effective than the short wave therapy.

Being tested
APOS - exercise component
Medical subject headings
Neck Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • APOS - exercise componentDevice

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. neck disability score

  2. neck pain score

  3. balance score

  4. cervical range of motion

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Dec 2005 (estimated)
  2. Study startMar 2006
  3. Study completionDec 2006 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Enrolment
132 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00266981
Sponsor's protocol ID
aposgo-HMO-CTIL
Status last verified
Dec 2005
First submitted
19 Dec 2005
Last updated
20 Dec 2005
Results posted
No

Questions about this trial

What is this clinical trial studying?

A study testing APOS - exercise component in people with Whiplash Associated Disorders and Cervical Pain, run by Hadassah Medical Organization at 1 site in Israel.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 20 Dec 2005. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Israel. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Goni Meron, PTB (00 972 2 5335039, goni_yehudai@walla.co.il), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

neck disability score. The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Dec 2005.

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