NCT02391740

Brief Summary

Describe the expectations of therapeutic education for patients in management of cancer pain.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
75

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2015

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2015

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

March 12, 2015

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 18, 2015

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2016

Completed
Last Updated

March 4, 2016

Status Verified

March 1, 2016

Enrollment Period

1 year

First QC Date

March 12, 2015

Last Update Submit

March 3, 2016

Conditions

Cancer

Outcome Measures

Primary Outcomes (1)

  • describe the expectations of therapeutic education for patients in management of cancer pain

    at inclusion

Secondary Outcomes (3)

  • Describe the expectations of close person in therapeutic education on management of cancer pain

    at inclusion

  • Estimate the intensity of the pain

    at inclusion

  • Estimate the echo of the pain on the daily activity of the patient

    at inclusion

Interventions

QuestionnaireOTHER

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients with cancer and pain

You may qualify if:

  • Patient with cancer diagnosed for at least one month
  • Patient with pain from the tumor or its treatment
  • Patients with a life expectancy ≥ 6 months
  • Health condition compatible with the requirements of the program (WHO performance scale \< or= 2)
  • Age over 18 years
  • Patient able to understand, speak and read French
  • Absence of cognitive impairment

You may not qualify if:

  • Primary cancer of the central nervous system or brain metastases
  • Disorders of the documented higher functions
  • Evolutionary psychiatric pathology
  • Drug User
  • Abusive alcohol consumption than the WHO recommendations (or 3 glasses of wine per day)
  • Refusal to participate

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

centre François Baclesse

Caen, France

Location

MeSH Terms

Conditions

Neoplasms

Interventions

Surveys and Questionnaires

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 12, 2015

First Posted

March 18, 2015

Study Start

February 1, 2015

Primary Completion

February 1, 2016

Study Completion

February 1, 2016

Last Updated

March 4, 2016

Record last verified: 2016-03

Locations

FR(1)