search
Back to results

Impact of Hypnosis Intervention on the Emotional Dimension of Dyspnea in Patients With COPD.

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Hypnosis intervention focused on the emotional dimension of the dyspnea
Sponsored by
5 Santé
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Obstructive Pulmonary Disease focused on measuring Dyspnea, Pulmonary rehabilitation, Physical activity, Hypnosis, Anxiety, COPD

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Admitted for a 4-week inpatient pulmonary rehabilitation program
  • COPD diagnosis with a value of the first second of forced expiration (FEV1) < 80% of theoretical values
  • 40 and 75 years old
  • Reading and writing skills

Exclusion Criteria:

  • Inability to answer a questionnaire
  • Patient with psychosis or psychiatric disorders with delusions (or delusions history)
  • Pregnant women
  • Protected adults
  • Participation in another study, with the exception of observational studies

Sites / Locations

  • Clinique du Souffle la VallonieRecruiting
  • Clinique du Souffle la Solane

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Hypnosis Arm

Control Arm

Arm Description

In parallel with an inpatient pulmonary rehabilitation program, nine visits will be carried out : V0 : an inclusion visit V1 : a randomization visit V2 to V6 : five visits with hypnosis sessions V7 : a end-stay visit V8 : a 6-month post-rehabilitation visit ( by phone call) The five hypnosis sessions (V2 to V6) will be spread over three weeks of rehabilitation program (1 to 2 hypnosis sessions per week). For V1, V7 and V8 : questionnaires will be filled about : quality of life (CAT questionnaire), the three dimensions of dyspnea (mMRC, LCADL and MDP questionnaires), anxiety and depression (HADS questionnaire), post-traumatic stress ( PCLS questionnaire), sedentarity and physical activity (SIMPAQ questionnaire). Other data will be also collected on : previous experiences with hypnosis, self-hypnosis and relaxation, number of exacerbations and hospitalizations in the past 6 months, drug treatment, psychotropic drug use and dosage and psychological follow-up.

In parallel with an inpatient pulmonary rehabilitation program, no additional intervention will be carry out and four visits will be carried out : V0 : an inclusion visit V1 : a randomization visit V7 : a end-stay visit V8 : a 6-month post-rehabilitation visit ( by phone call) For V1, V7 and V8 : questionnaires will be filled about : quality of life (CAT questionnaire), the three dimensions of dyspnea (mMRC, LCADL and MDP questionnaires), anxiety and depression (HADS questionnaire), post-traumatic stress ( PCLS questionnaire), sedentarity and physical activity (SIMPAQ questionnaire). Other data will be also collected on : previous experiences with hypnosis, self-hypnosis and relaxation, number of exacerbations and hospitalizations in the past 6 months, drug treatment, psychotropic drug use and dosage and psychological follow-up.

Outcomes

Primary Outcome Measures

Differential of the emotional dimension of dyspnea 6 months after pulmonary rehabilitation (PR)
Assessing differential of the emotional dimension of dyspnea score on the Multidimensional Dyspnea Profile scale (MDP questionnaire Meek et al 2012) 6 months after pulmonary rehabilitation (PR). MDP is a 11 items questionnaire. Each item is graded 0-10. 5 items are devoted to the emotional dimension of dyspnea. High scores indicate high prevalence of symptoms. As proposed by Morélot-Panzini et al in 2016, for filling it up, patient will be asked to focus on his worst dyspnea experience that happened oin the last two weeks.

Secondary Outcome Measures

Differential of the emotional dimension of dyspnea from baseline to PR end-stay and from PR end-stay to 6 months after PR
Assessing differential of the emotional dimension of dyspnea score on the Multidimensional Dyspnea Profile scale (MDP questionnaire Meek et al 2012) from baseline to PR end-stay and from PR end-stay to 6 months after PR . MDP is a 11 items questionnaire. Each item is graded 0-10. 5 items are devoted to the emotional dimension of dyspnea. High scores indicate high prevalence of symptoms. As proposed by Morélot-Panzini et al in 2016, for filling it up, patient will be asked to focus on his worst dyspnea experience that happened oin the last two weeks.
Differential of the impact dimension of dyspnea
Assessing differential of the impact dimension of dyspnea score on the modified Medical Research Council scale ( mMRC questionnaire) and on the London Chest of Activity Daily Living (LCADL) at the PR end-stay and 6 months after PR. mMRC is a 1 item questionnaire graded 0-4. High score indicates high prevalence of symptoms. LCADL is a15-item, self-administered questionnaire which allows an evaluation of dyspnea in patients with COPD during daily activities divided into four components: self-care, domestic, physical, and leisure. Patients could score from 0: "I would not do anyway" to 5: "I need someone else to do this". LCADL score is calculated by aggregating the points assigned to each question, with a higher score representing maximal disability.
Differential of the sensory dimension of dyspnea
Assessing differential of the sensory dimension of dyspnea score on the Multidimensional Dyspnea Profile scale (MDP questionnaire Meek et al 2012) at the PR end-stay and 6 months after PR. MDP is a 11 items questionnaire. Each item is graded 0-10. 6 items are devoted to the sensory dimension of dyspnea. High scores indicate high prevalence of symptoms. As proposed by Morélot-Panzini et al in 2016, for filling it up, patient will be asked to focus on his worst dyspnea experience that happened oin the last two weeks.
Differential of the post-traumatic stress disorder
Assessing differential of the post-traumatic stress disorder score (PCLS questionnaire) at the PR end-stay and 6 months after PR. PCLS is a 17 items questionnaire. Each item is graded 1-5. A score higher than 44 indicates patient has a post-traumatic disorder as defined by in Diagnostic and Statistical Manual of Mental Disorders IV (DSM IV) (Weathers et al, 1993).
Differential of the quality of life
Assessing differential of the quality of life score (COPD Assessment Test-CAT questionnaire) at the PR end-stay and 6 months after PR. CAT is a COPD specific questionnaire including 8 items. Each item is graded 0-5. Global score is comprised between 0 and 40. Higher global score is higher COPD impact on patient's quality of life is.
Differential of the anxiety and depression
Assessing differential of the anxiety and depression score (Hospital Anxiety and Depression Scale -HADS questionnaire) at the PR end-stay and 6 months after PR. HADS is a 14 items questionnaire (7 items for anxiety and 7 items for depression). Each item is graded 0-3. A score higher than 7 indicates anxiety and/or depression
Differential of the physical activity and sedentarity levels
Assessing differential of the physical activity and sedentarity levels (Simple Physical Activity Questionnaire (SIMPAQ) at the PR end-stay and 6 months after PR. SIMPAQ is a 5 items questionnaire assessing in the last two weeks physical activity levels, sedentary times and time in bed.
Questionnaire for assessing psychotropic drug quantity and dosage
A short questionnaire will be used for assessing differential of psychotropic drug quantity and dosage at the PR end-stay and 6 months after PR.
Number of exacerbations and hospitalizations
Assessing differential of number of exacerbations and hospitalizations 6 months after PR. Number of exacerbations and hospitalizations happened during the 6 last months will be indicated at T0 (baseline) and at T2 (6 month follow-up)
Hypnosis frequency
Assessing hypnosis frequency 6 months after PR.
Number of participants with previous hypnosis experiences
A questionnaire will be used for assessing patient's previous hypnosis experiences (previous to PR). (counting)
Self-Hypnosis frequency
Assessing self-hypnosis frequency 6 months after PR.
Number of participants with previous self-hypnosis experiences
A questionnaire will be used for assessing patient's previous self-hypnosis experiences (previous to PR). (counting)
Relaxation methods frequency
Assessing relaxation methods frequency 6 months after PR.
Number of participants with previous relaxation methods experiences
A questionnaire will be used for assessing patient's previous relaxation methods experiences (previous to PR). (counting)

Full Information

First Posted
June 26, 2019
Last Updated
January 16, 2023
Sponsor
5 Santé
search

1. Study Identification

Unique Protocol Identification Number
NCT04010825
Brief Title
Impact of Hypnosis Intervention on the Emotional Dimension of Dyspnea in Patients With COPD.
Official Title
Impact of Hypnosis Intervention Focused on the Emotional Dimension of Dyspnea on the Maintenance of Benefits for Patients With COPD After a Pulmonary Rehabilitation: A Multicenter Randomized Controlled Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 25, 2019 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
5 Santé

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the clinical study is to compare the effect of hypnosis intervention on the emotional dimension of the dyspnea during a pulmonary rehabilitation program to the pulmonary rehabilitation program alone. This study will determine if the hypnosis intervention will lead to better maintenance of benefits obtained than the original described method.
Detailed Description
While physical activity level is the best predictor of life expectancy for patients with chronic obstructive pulmonary disease (COPD), the majority of patients have physical activity levels well below guidelines. One of the main barriers to regular activity is anxiety related to dyspnea. Defined as a subjective experience of discomfort during breathing, dyspnea is described as a multidimensional phenomenon integrating both the impact dimension (daily disability), the sensory dimension (intensity of dyspnea) and the emotional dimension (unpleasant and anxiety-aspects). The most effective treatment to reduce dyspnea is pulmonary rehabilitation. An overall improvement in dyspnea, and more specifically in its emotional dimension, has been achieved by reducing dyspnea anxiety. By reducing one of the major barriers to regular physical activity, the level of post-rehabilitation physical activity should also be improved. However, paradoxically, many studies have reported that there has been no change in the level of physical activity of patients in post-rehabilitation. A possible hypothesis to explain this decoupling between the improvement of the emotional dimension of dyspnea and the absence of behavioral modification, lies in the disappearance of the effects once at home. Indeed, during a pulmonary rehabilitation stay, patients practice under health professionals' supervision and advices with regular feedback on their abilities. When patients return home left on their own again, dyspnea anxiety is likely to reappear and motivation may not be enough. Several techniques have been proposed to complement traditional interventions in order to strengthen rehabilitation effects. Unfortunately, these are not effective. The use of hypnosis as a complement to rehabilitation programs is a promising perspective to maintain the benefits on the emotional dimension of dyspnea after a rehabilitation program. Its benefits have already been demonstrated in the reduction of acute and chronic pains, in a long-term effectiveness using self-hypnosis techniques. These ensure the continuity of remote management of the intervention. Given the analogy between pain and dyspnea, hypnosis could therefore constitute a therapeutic solution as a complement to rehabilitation to durably reduce dyspnea anxiety in patients with COPD, and promote a better behavior at middle and long term. The investigators hypothesize that hypnosis used in addition to a 4-week pulmonary rehabilitation program will maintain the benefits on the emotional dimension of dyspnea at 6 months in the experimental group compared to a control group. The main objective is to evaluate the impact of a hypnosis intervention during a pulmonary rehabilitation program on the emotional dimension of dyspnea 6 months after patients return home (T2).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
Dyspnea, Pulmonary rehabilitation, Physical activity, Hypnosis, Anxiety, COPD

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
106 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hypnosis Arm
Arm Type
Experimental
Arm Description
In parallel with an inpatient pulmonary rehabilitation program, nine visits will be carried out : V0 : an inclusion visit V1 : a randomization visit V2 to V6 : five visits with hypnosis sessions V7 : a end-stay visit V8 : a 6-month post-rehabilitation visit ( by phone call) The five hypnosis sessions (V2 to V6) will be spread over three weeks of rehabilitation program (1 to 2 hypnosis sessions per week). For V1, V7 and V8 : questionnaires will be filled about : quality of life (CAT questionnaire), the three dimensions of dyspnea (mMRC, LCADL and MDP questionnaires), anxiety and depression (HADS questionnaire), post-traumatic stress ( PCLS questionnaire), sedentarity and physical activity (SIMPAQ questionnaire). Other data will be also collected on : previous experiences with hypnosis, self-hypnosis and relaxation, number of exacerbations and hospitalizations in the past 6 months, drug treatment, psychotropic drug use and dosage and psychological follow-up.
Arm Title
Control Arm
Arm Type
No Intervention
Arm Description
In parallel with an inpatient pulmonary rehabilitation program, no additional intervention will be carry out and four visits will be carried out : V0 : an inclusion visit V1 : a randomization visit V7 : a end-stay visit V8 : a 6-month post-rehabilitation visit ( by phone call) For V1, V7 and V8 : questionnaires will be filled about : quality of life (CAT questionnaire), the three dimensions of dyspnea (mMRC, LCADL and MDP questionnaires), anxiety and depression (HADS questionnaire), post-traumatic stress ( PCLS questionnaire), sedentarity and physical activity (SIMPAQ questionnaire). Other data will be also collected on : previous experiences with hypnosis, self-hypnosis and relaxation, number of exacerbations and hospitalizations in the past 6 months, drug treatment, psychotropic drug use and dosage and psychological follow-up.
Intervention Type
Other
Intervention Name(s)
Hypnosis intervention focused on the emotional dimension of the dyspnea
Intervention Description
Individual hypnosis sessions will be for 1 hour. Each hypnosis session will be standardized and evaluated using a script and an observation grid ( Visual Analogic Scale comfort, patient's hypnotic state...) written in collaboration with experts from Institut Milton Hyland Erickson Toulouse France (IMHETO).
Primary Outcome Measure Information:
Title
Differential of the emotional dimension of dyspnea 6 months after pulmonary rehabilitation (PR)
Description
Assessing differential of the emotional dimension of dyspnea score on the Multidimensional Dyspnea Profile scale (MDP questionnaire Meek et al 2012) 6 months after pulmonary rehabilitation (PR). MDP is a 11 items questionnaire. Each item is graded 0-10. 5 items are devoted to the emotional dimension of dyspnea. High scores indicate high prevalence of symptoms. As proposed by Morélot-Panzini et al in 2016, for filling it up, patient will be asked to focus on his worst dyspnea experience that happened oin the last two weeks.
Time Frame
Change from baseline (T0) to 6 month follow-up (T2)
Secondary Outcome Measure Information:
Title
Differential of the emotional dimension of dyspnea from baseline to PR end-stay and from PR end-stay to 6 months after PR
Description
Assessing differential of the emotional dimension of dyspnea score on the Multidimensional Dyspnea Profile scale (MDP questionnaire Meek et al 2012) from baseline to PR end-stay and from PR end-stay to 6 months after PR . MDP is a 11 items questionnaire. Each item is graded 0-10. 5 items are devoted to the emotional dimension of dyspnea. High scores indicate high prevalence of symptoms. As proposed by Morélot-Panzini et al in 2016, for filling it up, patient will be asked to focus on his worst dyspnea experience that happened oin the last two weeks.
Time Frame
Changes from baseline (T0) to at the end of the 4-weeks PR (T1) and from T1 to 6 month follow-up (T2)
Title
Differential of the impact dimension of dyspnea
Description
Assessing differential of the impact dimension of dyspnea score on the modified Medical Research Council scale ( mMRC questionnaire) and on the London Chest of Activity Daily Living (LCADL) at the PR end-stay and 6 months after PR. mMRC is a 1 item questionnaire graded 0-4. High score indicates high prevalence of symptoms. LCADL is a15-item, self-administered questionnaire which allows an evaluation of dyspnea in patients with COPD during daily activities divided into four components: self-care, domestic, physical, and leisure. Patients could score from 0: "I would not do anyway" to 5: "I need someone else to do this". LCADL score is calculated by aggregating the points assigned to each question, with a higher score representing maximal disability.
Time Frame
Changes from baseline (T0) to at the end of the 4-weeks PR (T1) , from T0 to 6 month follow-up (T2) and from T1 to 6 month follow-up (T2)
Title
Differential of the sensory dimension of dyspnea
Description
Assessing differential of the sensory dimension of dyspnea score on the Multidimensional Dyspnea Profile scale (MDP questionnaire Meek et al 2012) at the PR end-stay and 6 months after PR. MDP is a 11 items questionnaire. Each item is graded 0-10. 6 items are devoted to the sensory dimension of dyspnea. High scores indicate high prevalence of symptoms. As proposed by Morélot-Panzini et al in 2016, for filling it up, patient will be asked to focus on his worst dyspnea experience that happened oin the last two weeks.
Time Frame
Changes from baseline (T0) to at the end of the 4-weeks PR (T1) , from T0 to 6 month follow-up (T2) and from T1 to 6 month follow-up (T2)
Title
Differential of the post-traumatic stress disorder
Description
Assessing differential of the post-traumatic stress disorder score (PCLS questionnaire) at the PR end-stay and 6 months after PR. PCLS is a 17 items questionnaire. Each item is graded 1-5. A score higher than 44 indicates patient has a post-traumatic disorder as defined by in Diagnostic and Statistical Manual of Mental Disorders IV (DSM IV) (Weathers et al, 1993).
Time Frame
Changes from baseline (T0) to at the end of the 4-weeks PR (T1) , from T0 to 6 month follow-up (T2) and from T1 to 6 month follow-up (T2)
Title
Differential of the quality of life
Description
Assessing differential of the quality of life score (COPD Assessment Test-CAT questionnaire) at the PR end-stay and 6 months after PR. CAT is a COPD specific questionnaire including 8 items. Each item is graded 0-5. Global score is comprised between 0 and 40. Higher global score is higher COPD impact on patient's quality of life is.
Time Frame
Changes from baseline (T0) to at the end of the 4-weeks PR , from T0 to 6 month follow-up (T2) and from T1 to 6 month follow-up (T2)
Title
Differential of the anxiety and depression
Description
Assessing differential of the anxiety and depression score (Hospital Anxiety and Depression Scale -HADS questionnaire) at the PR end-stay and 6 months after PR. HADS is a 14 items questionnaire (7 items for anxiety and 7 items for depression). Each item is graded 0-3. A score higher than 7 indicates anxiety and/or depression
Time Frame
Changes from baseline (T0) to at the end of the 4-weeks PR (T1) , from T0 to 6 month follow-up (T2) and from T1 to 6 month follow-up (T2)
Title
Differential of the physical activity and sedentarity levels
Description
Assessing differential of the physical activity and sedentarity levels (Simple Physical Activity Questionnaire (SIMPAQ) at the PR end-stay and 6 months after PR. SIMPAQ is a 5 items questionnaire assessing in the last two weeks physical activity levels, sedentary times and time in bed.
Time Frame
Changes from baseline (T0) to at the end of the 4-weeks PR (T1) , from T0 to 6 month follow-up (T2) and from T1 to 6 month follow-up (T2)
Title
Questionnaire for assessing psychotropic drug quantity and dosage
Description
A short questionnaire will be used for assessing differential of psychotropic drug quantity and dosage at the PR end-stay and 6 months after PR.
Time Frame
Changes from baseline (T0) to at the end of the 4-weeks PR (T1) , from T0 to 6 month follow-up (T2) and from T1 to 6 month follow-up (T2)
Title
Number of exacerbations and hospitalizations
Description
Assessing differential of number of exacerbations and hospitalizations 6 months after PR. Number of exacerbations and hospitalizations happened during the 6 last months will be indicated at T0 (baseline) and at T2 (6 month follow-up)
Time Frame
Changes from baseline (T0) to 6 month follow-up (T2)
Title
Hypnosis frequency
Description
Assessing hypnosis frequency 6 months after PR.
Time Frame
Changes from baseline (T0) to 6 month follow-up (T2)
Title
Number of participants with previous hypnosis experiences
Description
A questionnaire will be used for assessing patient's previous hypnosis experiences (previous to PR). (counting)
Time Frame
Months or/and years before PR baseline (T0)
Title
Self-Hypnosis frequency
Description
Assessing self-hypnosis frequency 6 months after PR.
Time Frame
Changes from baseline (T0) to 6 month follow-up (T2)
Title
Number of participants with previous self-hypnosis experiences
Description
A questionnaire will be used for assessing patient's previous self-hypnosis experiences (previous to PR). (counting)
Time Frame
Months or/and years before PR baseline (T0)
Title
Relaxation methods frequency
Description
Assessing relaxation methods frequency 6 months after PR.
Time Frame
Changes from baseline (T0) to 6 month follow-up (T2)
Title
Number of participants with previous relaxation methods experiences
Description
A questionnaire will be used for assessing patient's previous relaxation methods experiences (previous to PR). (counting)
Time Frame
Months or/and years before PR baseline (T0)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Admitted for a 4-week inpatient pulmonary rehabilitation program COPD diagnosis with a value of the first second of forced expiration (FEV1) < 80% of theoretical values 40 and 75 years old Reading and writing skills Exclusion Criteria: Inability to answer a questionnaire Patient with psychosis or psychiatric disorders with delusions (or delusions history) Pregnant women Protected adults Participation in another study, with the exception of observational studies
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nelly Heraud, PhD
Phone
+33 4 67 88 84 91
Email
nelly.heraud@korian.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adriana Castanyer
Organizational Affiliation
5 SANTE - Clinique du Souffle la Solane
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nelly Heraud, PhD
Organizational Affiliation
5 Santé
Official's Role
Study Director
Facility Information:
Facility Name
Clinique du Souffle la Vallonie
City
Lodève
ZIP/Postal Code
34700
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nathalie Fernandes
Phone
+33467888470
Email
nathalie.fernandes@inicea.fr
Facility Name
Clinique du Souffle la Solane
City
Osséja
ZIP/Postal Code
66340
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Adriana Castanyer
Phone
+33468308490
Email
adriana.castanyer@inicea.fr

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Impact of Hypnosis Intervention on the Emotional Dimension of Dyspnea in Patients With COPD.

We'll reach out to this number within 24 hrs