PSYCANCER: EMDR Psychotherapy for Anxious-depressive Symptoms in Breast Cancer Patient

Sponsor
Centre Hospitalier Régional Metz-Thionville (Other)
Overall Status
Recruiting
CT.gov ID
NCT03898453
Collaborator
University of Lorraine (Other), Central Hospital, Nancy, France (Other)
190
1
2
63
3

Study Details

Study Description

Brief Summary

The study will consist in an evaluation of the EMDR (Eye Movement Desensitization and Reprocessing) psychotherapy in the context on invasive primitive breast cancer. EMDR could then allow the affected patients to readjust their point of view on the pathology and thus promote more adapted behaviors or additional resources to cope with the disease. 190 Patients are going to be randomized in two groups : one group with EMDR psychotherapists and one group with support psychotherapists. Patients will receive 8 sessions. We expect that patient in EMDR psychotherapists group will have an higher decrease of anxiety score, depressive score (CES-D) and PTSD score, and a higher increase in quality of life.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: EMDR psychotherapy
  • Behavioral: support psychotherapy
N/A

Detailed Description

The study will consist in an evaluation of the EMDR psychotherapy in the context on invasive primitive breast cancer. EMDR could then allow the affected patients to readjust their point of view on the pathology and thus promote more adapted behaviors or additional resources to cope with the disease. 190 Patients are going to be randomized in two groups : one group with EMDR psychotherapists and one group with support psychotherapists. Patients will receive 8 sessions. We expect that patient in EMDR psychotherapists group will have an higher decrease of anxiety score, depressive score and PTSD score, and a higher increase in quality of life (QLQ)

Study Design

Study Type:
Interventional
Anticipated Enrollment :
190 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Two groups assignment - One group will receive EMDR psychotherapy the other one support psychotherapy.Two groups assignment - One group will receive EMDR psychotherapy the other one support psychotherapy.
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
EMDR Psychotherapy of Anxious-depressive Symptoms for Women That Present an Invasive Breast Cancer : a Randomised Controlled Trial
Actual Study Start Date :
Nov 5, 2018
Anticipated Primary Completion Date :
Nov 5, 2022
Anticipated Study Completion Date :
Feb 5, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group EMDR psychotherapy

Visit 0 : patient inclusion (questionnaires and interview) Visit 1 : anamnesis Visit 2 : patient stabilisation Visit 3 : EMDR psychotherapy care Visit 4 : EMDR psychotherapy care Visit 5 : EMDR psychotherapy care and questionnaires Visit 6 : EMDR psychotherapy care Visit 7 : EMDR psychotherapy care and questionnaires Follow-up 8 (three month after) : data recovery (questionnaires) Follow-up 9 (six month after) : data recovery (questionnaires)

Behavioral: EMDR psychotherapy
Visit 0 : patient inclusion (questionnaires and interview) Visit 1 : anamnesis Visit 2 : patient stabilisation Visit 3 : EMDR psychotherapy care Visit 4 : EMDR psychotherapy care Visit 5 : EMDR psychotherapy care and questionnaires Visit 6 : EMDR psychotherapy care Visit 7 : EMDR psychotherapy care and questionnaires Follow-up 8 (three month after) : data recovery (questionnaires) Follow-up 9 (six month after) : data recovery (questionnaires)

Other: Group Control : support psychotherapy

Visit 0 : patient inclusion (questionnaires and interview) Visits 1-7: several methods could be used: psychoeducation about cancer and psychotherapy, positive interaction and activity schedule, emotional support , relaxation, prevention techniques… Questionnaires will be completed by patients at visit 5 and 7. Follow-up 8 (one month after) : data recovery (questionnaires) Follow-up 9 (six month after) : data recovery (questionnaires)

Behavioral: support psychotherapy
Visit 0 : patient inclusion (questionnaires and interview) Visits 1-7: several methods could be used: psychoeducation about cancer and psychotherapy, positive interaction and activity schedule, emotional support , relaxation, prevention techniques… Questionnaires will be completed by patients at visit 5 and 7. Follow-up 8 (one month after) : data recovery (questionnaires) Follow-up 9 (six month after) : data recovery (questionnaires)

Outcome Measures

Primary Outcome Measures

  1. State Anxiety [Month 9]

    STAI-Y-A (State-Trait Anxiety Inventory) This questionnaire consists of a 20-items. The state version (STAI Y-A) indicate for 20 items and on 4-point Likert-Scale (not at all, somewhat, moderately so, and very much so) the extent to which they are currently experiencing each symptoms of anxiety. The total score ranges from 20 to 80. A higher total score indicate a higher level of anxiety.

Secondary Outcome Measures

  1. quality of life of cancer patients [Month 9]

    EORTC QLQ-C30 Questionnaire The European Organization for research and Treatment of Cancer 30-item Quality of life (QoL) questionnaire is a well-validated health-related QoL instrument.

  2. depression [Month 9]

    CES-D (The Center for Epidemiologic Studies Depression) Questionnaire

  3. posttraumatic symptoms [Month 9]

    PTGI (The Posttraumatic Growth Inventory) Questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Being a 18 or more year old woman

  • Having primary breast cancer or going to start treatment or having completed treatments for less than 6 months

  • Presenting a state-anxiety level a score higher than 35.

  • Being able to complete questionnaires.

  • Having signed the consent letter

  • Be affiliated to a social security system

Exclusion Criteria:
  • Have contraindications for EMDR psychotherapy (neurological disorders, dissociative states, oculomotor problems)

  • Have metastatic breast cancer

  • physical multiple pathologies

  • Have a psychiatric history (including anxio-depressive disorders). Background Assessment from M.I.N.I. (Sheehan et al., 1997)

  • Present an addiction, an abuse of drugs or alcohol

  • Person placed under the protection of justice, guardianship or trusteeship.

  • Pregnant or lactating woman

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHR Metz-Thionville Metz France 57085

Sponsors and Collaborators

  • Centre Hospitalier Régional Metz-Thionville
  • University of Lorraine
  • Central Hospital, Nancy, France

Investigators

  • Principal Investigator: Raffaele LONGO, Dr, CHR Metz-Thionville

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Régional Metz-Thionville
ClinicalTrials.gov Identifier:
NCT03898453
Other Study ID Numbers:
  • 2018-A01128-47
First Posted:
Apr 2, 2019
Last Update Posted:
Sep 13, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Centre Hospitalier Régional Metz-Thionville
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 13, 2021