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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02367079
Other study ID # StudiFM
Secondary ID
Status Terminated
Phase Phase 4
First received January 21, 2015
Last updated February 12, 2015
Start date April 2014
Est. completion date April 2014

Study information

Verified date February 2015
Source Studi Fisioterapici di Montagna
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Interventional

Clinical Trial Summary

To investigate the effect of hand massage, switched on diathermy or sham/switched off diathermy on DOMS in a group of athletes suffering DOMS after a ski mountaineering race.


Description:

This study examine DOMS in athletes following a ski mountaineering race, pain measured with numbering pain rating scale NPRS and perceived global improvement (PGIC) after treatment have been measured after a massage treatment, a diathermy treatment and a sham diathermy treatment.


Recruitment information / eligibility

Status Terminated
Enrollment 25
Est. completion date April 2014
Est. primary completion date April 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria:

- Healthy patients who complaints about D.O.M.S. after a skimountaneering race

Exclusion Criteria:

- Patient who complain of pathology such trauma or declaring consuming drugs for pain management where excluded from the study.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Diathermy
Sham diathermy vs switched on diathermy effect on pain where assessed

Locations

Country Name City State
Italy Studi fisioterapici di Montagna Aosta

Sponsors (1)

Lead Sponsor Collaborator
Studi Fisioterapici di Montagna

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Numering pain rating scale Numering pain rating scale was assessed pre e post treatment Day 1 Yes
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