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Evaluation of Depression In Chronic Obstructive Pulmonary Disease (EDIC)

Primary Purpose

Depression in Patients With Chronic Obstructive Pulmonary Disease

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Aerobic Exercise
Sponsored by
University Hospital, Catania
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression in Patients With Chronic Obstructive Pulmonary Disease focused on measuring Depression, COPD, Aerobic Exercise, Anxiety, Quality of life, neurocognitive functioning

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Diagnosis of COPD and depression, eligibility to perform pulmonary rehabilitation according to ATS and ERS guidelines.

Exclusion Criteria:

indication to restoring treatment of airway patency and current psychopharmacological treatment (including sleeping-pills).

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    No Intervention

    Arm Label

    Aerobic exercise

    Control sample

    Arm Description

    A six week aerobic exercise intervention in COPD depressed population.

    Only participants randomized in the arm named "Aerobic exercise" will receive a six weeks aerobic exercise intervention.

    Outcomes

    Primary Outcome Measures

    variation of HDRS total score
    we compare the variation of HDRS total score, as primary outcome measure, in two groups (A, B) of COPD depressed patients matched for: COPD status; depressive status; age; gender. Only the participants randomized in study group A will receive a 6-weeks aerobic exercise intervention.

    Secondary Outcome Measures

    daily functioning assessment
    Evaluation of potential benefits on: anxiety symptoms, cognitive features, daily physical function (related to physical performances and/or to psychopathological dimensions) and quality of life.

    Full Information

    First Posted
    May 22, 2014
    Last Updated
    May 27, 2014
    Sponsor
    University Hospital, Catania
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02147912
    Brief Title
    Evaluation of Depression In Chronic Obstructive Pulmonary Disease
    Acronym
    EDIC
    Official Title
    Evaluation of Depression In Chronic Obstructive Pulmonary Disease: a Longitudinal Randomized Controlled Trial.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2014
    Overall Recruitment Status
    Unknown status
    Study Start Date
    November 2014 (undefined)
    Primary Completion Date
    May 2015 (Anticipated)
    Study Completion Date
    November 2015 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University Hospital, Catania

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Background: Several clinical studies show high rates of anxiety and depressive disorders in Chronic Obstructive Pulmonary Disease (COPD), that suggest common underlying pathogenetic mechanisms of COPD and depressive disorders. The aim of this study is to evaluate the effects of aerobic exercise, proposed in the context of pulmonary rehabilitation, in a sample of COPD depressed patients without psychopharmacological treatment, through the correlation of some psychopathological variables and physical/pneumological parameters. Methods: The investigators have designed an observational longitudinal trial. The trial will be prospective 6-weeks randomized clinical study to evaluate the impact of aerobic exercise on depressive symptoms in 154 patient affected by COPD and depression, assessed by Hamilton Depression Rating Scale (HDRS). The investigators will also monitor anxiety, quality of life and neurocognitive function. Outcome measures: The investigators compare the variation of HDRS total score, as primary outcome measure, in two groups (A, B) of COPD depressed patients matched for: COPD status; depressive status; age; gender. Only the participants randomized in study group A will receive a 6-weeks aerobic exercise intervention. Statistical analysis: All tests are two-tailed and a p value 0.05 was considered significant. The difference between the two groups will be evaluated with Student's T test for normally distributed data, and with Mann-Whitney's U test, for those with not normal distribution. The normality of distribution will be evaluated with the Kolmogorov-Smirnov test. Any correlations among the variables under evaluation will be assessed by Spearman r correlation. Variables will be compared using the Chi-squared test or Fisher exact test for categorical variables. Discussion: There is a strong correlation between physical activity and mental health. Several data have suggested that aerobic exercise shows significant effects, comparable to pharmacotherapy and to psychotherapy, on reducing depressive symptomatology. The goal of our study is to propose an effective intervention to reduce the risk of severe depression in this special population, evaluating the variation of HDRS total score after the aerobic exercise intervention.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Depression in Patients With Chronic Obstructive Pulmonary Disease
    Keywords
    Depression, COPD, Aerobic Exercise, Anxiety, Quality of life, neurocognitive functioning

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    154 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Aerobic exercise
    Arm Type
    Active Comparator
    Arm Description
    A six week aerobic exercise intervention in COPD depressed population.
    Arm Title
    Control sample
    Arm Type
    No Intervention
    Arm Description
    Only participants randomized in the arm named "Aerobic exercise" will receive a six weeks aerobic exercise intervention.
    Intervention Type
    Other
    Intervention Name(s)
    Aerobic Exercise
    Intervention Description
    Aerobic exercise intervention consists of lower (treadmill and cyclette) and upper arts (arm ergometer Davenbike®) training, as well as calisthenic exercises with increasing intensity from a minimum of 80% to a maximum workload for lower arts in a minimum time.
    Primary Outcome Measure Information:
    Title
    variation of HDRS total score
    Description
    we compare the variation of HDRS total score, as primary outcome measure, in two groups (A, B) of COPD depressed patients matched for: COPD status; depressive status; age; gender. Only the participants randomized in study group A will receive a 6-weeks aerobic exercise intervention.
    Time Frame
    6 weeks after intervention phase
    Secondary Outcome Measure Information:
    Title
    daily functioning assessment
    Description
    Evaluation of potential benefits on: anxiety symptoms, cognitive features, daily physical function (related to physical performances and/or to psychopathological dimensions) and quality of life.
    Time Frame
    6 weeks after intervention phase

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    40 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosis of COPD and depression, eligibility to perform pulmonary rehabilitation according to ATS and ERS guidelines. Exclusion Criteria: indication to restoring treatment of airway patency and current psychopharmacological treatment (including sleeping-pills).
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Giuseppe Minutolo, MD, PhD
    Phone
    +39 0953782791
    Email
    giuseppeminutolo@hotmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Francesca Magnano S. Lio, MD
    Phone
    +39 0953782470
    Email
    francesca.magnanosanlio@gmail.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Eugenio Aguglia, Prof.
    Organizational Affiliation
    UOPI of psychiatry - Department of clinical and molecular biomedicine - AOU Policlinico-Vittorio Emanuele. Via S. Sofia, 78 - 95124 Catania, Italy
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Giuseppe Minutolo, MD, PhD
    Organizational Affiliation
    UOPI of psychiatry - Department of clinical and molecular biomedicine - AOU Policlinico-Vittorio Emanuele. Via S. Sofia, 78 - 95124 Catania, Italy
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Giuseppe Catalfo, MD
    Organizational Affiliation
    UOPI of psychiatry - Department of clinical and molecular biomedicine - AOU Policlinico-Vittorio Emanuele. Via S. Sofia, 78 - 95124 Catania, Italy
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Francesca Magnano S. Lio, MD
    Organizational Affiliation
    UOPI of psychiatry - Department of clinical and molecular biomedicine - AOU Policlinico-Vittorio Emanuele. Via S. Sofia, 78 - 95124 Catania, Italy
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Nunzio Crimi, Prof.
    Organizational Affiliation
    Pulmonary Rehabilitation Clinic - Department of clinical and molecular biomedicine - AOU Policlinico-Vittorio Emanuele. Via S. Sofia, 78 - 95124 Catania, Italy
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Evaluation of Depression In Chronic Obstructive Pulmonary Disease

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