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Measuring the Effects of Touch Relaxation Painful Patients in Oncologie Nursing (ToucherDétente)

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ClinicalTrials.gov Identifier: NCT02857114
Recruitment Status : Unknown
Verified July 2016 by Assistance Publique Hopitaux De Marseille.
Recruitment status was:  Recruiting
First Posted : August 5, 2016
Last Update Posted : August 5, 2016
Sponsor:
Information provided by (Responsible Party):
Assistance Publique Hopitaux De Marseille

Brief Summary:
Measure the impact of touch relaxation on pain communicative patients suffering from chronic pain of cancer origin inpatient Oncology. measure over three days the effects on pain anxiety welfare and consumption of analgesics

Condition or disease Intervention/treatment Phase
Cancer Other: massage Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 104 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Study Start Date : February 2015
Estimated Primary Completion Date : February 2018
Estimated Study Completion Date : December 2018

Arm Intervention/treatment
massage Other: massage



Primary Outcome Measures :
  1. Pain [ Time Frame: 3 days ]
    pain measurement by the scale numerical pain


Secondary Outcome Measures :
  1. anxiety [ Time Frame: 3 days ]
    measurement with the scale of COVI

  2. consumption of analgesics [ Time Frame: 3 days ]
    daily creel analgesics and anxiolytics

  3. wellness [ Time Frame: 3 days ]
    measure with the scale of edmonton



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

hospitalized in the oncology department at least 3 days

  • presenting the cancerous type of pain caused by their disease or treatment
  • numerical scale pain score = 4/10
  • receiving weak and strong opioids
  • platelet count> 100
  • can receive anxiolytic
  • adult
  • Patient of both sexes
  • no other relaxation approaches

Exclusion Criteria:

  • against indication to touch: wound, bruises, circulatory disorders, diseases psychiatiques
  • risk of hematoma
  • numerical scale pain score < 4/10
  • understanding of the difficulties of the French language
  • no receiving weak and strong opioids

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02857114


Contacts
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Contact: Michelle GAIDE 04 91 38 27 47 drci@ap-hm.fr

Locations
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France
Hôpital de la Timone Assistance Publique Hôpitaux de Marseille Recruiting
Marseille, France, 13354
Contact: Michelle GAIDE    0491382747    drci@ap-hm.fr   
Sponsors and Collaborators
Assistance Publique Hopitaux De Marseille
Investigators
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Study Director: Urielle DESALBRES Assistance Publique Hôpitaux de Marseille
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Responsible Party: Assistance Publique Hopitaux De Marseille
ClinicalTrials.gov Identifier: NCT02857114    
Other Study ID Numbers: 2014-20
First Posted: August 5, 2016    Key Record Dates
Last Update Posted: August 5, 2016
Last Verified: July 2016