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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05493150
Other study ID # 00006
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 22, 2020
Est. completion date December 30, 2021

Study information

Verified date August 2022
Source Centre Hospitalier de Valence
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

observational , Monocentric, study to assess antalgic effects of well-being treatment in cancer care.


Description:

Contrary to supportive care, well-being care is imperfectly assessed. Well being care (WBC) consist on complementary programs, with no real consensus. Very few studies have rigorously evaluated its benefits The objective of this study was to evaluate the impact of four well-being treatments (foot reflexology, socio-aesthetics, Sophrology and singing) provided in a healthcare facility


Recruitment information / eligibility

Status Completed
Enrollment 180
Est. completion date December 30, 2021
Est. primary completion date September 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - all type of cancer treated at the general Hospital of Valence - patient agree to participate on Well being session: foot reflexology, socio-aesthetics, Sophrology and singing - Age = 18 years - Affiliation to a Social security system - Patient who has given written consent signed before any specific procedure of the protocol Exclusion Criteria: - Patient under guardianship, deprived of liberty, safeguard of justice - Patient presenting a serious psychiatric pathology that does not allow compliance with the completion of the scale (at the discretion of the investigator) - Refusal to participate in research

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Ch Valence Valence Drome

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier de Valence

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain assesment numerical scale 0 to 10, with 0 being "no pain" and 10 being "the worst pain imaginable." 1 immediately before well being treatment
Primary Pain assesment numerical scale 0 to 10, with 0 being "no pain" and 10 being "the worst pain imaginable." 1 immediately after well being treatment
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