- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01543815
Well-Being Therapy by Personalized Mobile Technology Program for Psychological Distress and Promote Healthy Behaviors (WELL-ME)
March 4, 2012 updated by: Angelo Compare, University of Bergamo
Well-Being Therapy for Psychological Distress and Enhancing Healthy Behaviors With Personalized Mobile Technology in Cardiac Patients: a Randomized Controlled-trial Study Protocol
The WELL-ME study is a three-arm randomized controlled clinical trial (RCT).
The aim of this RCT is to compare the effectiveness of the Well Being Web Based Therapy (WBT-Web) with the gold standard CBT (Cognitive Behavior Therapy) and standard clinical procedure of patients' management (CM) for psychological distress and promotion of healthy behaviors in Cardiac Patients.
Study Overview
Status
Completed
Conditions
Detailed Description
Cardiac disease (CD) affects millions of European and Americans and new diagnosis rates are expected to almost triple over the next 30 years as our population ages.
Affective disorders including clinical depression, anxiety and psychological distress are common in patients with CD.
Furthermore, the presence of these disorders significantly impacts quality of life, adherence to medical prescription and healthy behaviors.
The prevalence of depression, ranging from 11% to 25% among heart disease outpatients and 35% to 70% among those who are hospitalized.
Psychological depression appears to be an important predictor of rehospitalization among persons who have been admitted with coronary artery disease.
In addition, depression in patients with heart failure was found to be associated with the course of the disease and its prognosis.
The high prevalence of psychological distress among the population of patients with heart failure, along with the broad impact on the patient's quality of life, requires attention to detail and the implementation of interventions aimed at reducing levels of distress.
Very few studies describe interventions aimed at alleviating distress in patients with heart failure.
Cognitive Behavioral Therapy (CBT) is reported to improve both the functional and emotional levels of these patients, resulting in the relief of their symptoms of depression.
Recently Well Being Therapy WBT) have showed promising outcomes findings for depression and distress.
There is a need to treat patients in their real life setting.
Recent technological innovations in the ICT provide to monitor and treat the patient at a distance outside the hospital.
The aim in this study is to study the effectiveness of the WBT-WEB in reducing psychological distress, and improving QoL, healthy behaviors and medical adherence in HR compared to a CBT and standard clinical procedure of patients' management (CM).
The same protocol will be carried out in two centres (Hospital de Terrassa, Barcelona, Spain; National and Kapodistrian University of Athens, Greece).
300 patients diagnosed with cardiac disease, and with psychological distress, assessed by Hospital Anxiety and Depression Scale (HADS) will be randomized to one of three treatment groups: 1) WBT-WEB; 2) CBT and 3) CM.
A one-year follow-up will be performed.
It is expected that WBT-WEB may significantly decrease psychological distress and increase QoL, healthy behaviors and medical adherence at follow-up compared to clinical management.
Study Type
Interventional
Enrollment (Actual)
400
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Cardiac Diseases
- a current diagnosis of at least one of the following: major or minor depression, dysthymia, anxiety according, to DSM-IV criteria, and HADS criteria
- Mini-Mental State Examination score higher than 24
- written informed consent provided by the patient to participate
Exclusion Criteria:
- uncertain prognosis for 12 months due to other conditions
- acute coronary disease in recent months.
- existence of another life-threatening illness of the patient (such as active cancer, chronic kidney failure).
- severe neurological problem (Brain syndrome / orientation problem/ difficult peripheral neuropathy).
- severe mental illness (active psychosis / suicide risk / severe dementia).
- linguistic limitations (such as stuttering / untreated audio impairment).
- a significant functional problem (such as unconsciousness / connection to respiration device / confined to a wheelchair or bed / severe walking disability / needs help with complete basic daily activities).
- objective limit that endangers liability for participation in the seven meetings (such as remote residential / tourist / convict / drug addict).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: WBT-WEB
Well-Being Therapy based on Web Mobile technology
|
The techniques included in WBT may be used in overcoming impairments in environmental mastery, purpose in life, personal growth, autonomy, self-acceptance and positive relations with others.
|
|
Active Comparator: CBT
Cognitive Behavior Therapy
|
CBT involves several essential features: identifying and correcting inaccurate thoughts associated with depressed feelings (cognitive restructuring); helping patients to engage more often in enjoyable activities (behavioral activation); enhancing problem-solving skills; providing instruction and guidance in specific strategies for solving problems.
|
|
No Intervention: CM
Standardized Care Management
|
CM will consist of reviewing the patients' clinical status, and providing the patient with support and advice if necessary.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Psychological distress
Time Frame: Within one year after the treatment
|
Depression, Anxiety, and well-being improvements (Psychological Distress Reduction)
|
Within one year after the treatment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of Life
Time Frame: Within one year after the treatment
|
Quality of Life
|
Within one year after the treatment
|
|
Medical Adherence
Time Frame: Within one year after the treatment
|
Within one year after the treatment
|
|
|
Promotion of Healthy Lifestyle
Time Frame: Within one year after the treatment
|
Promotion of Healthy Lifestyle
|
Within one year after the treatment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Angelo Compare, Ph.D, University of Bergamo
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2006
Primary Completion (Actual)
February 1, 2009
Study Completion (Actual)
December 1, 2010
Study Registration Dates
First Submitted
February 28, 2012
First Submitted That Met QC Criteria
March 2, 2012
First Posted (Estimate)
March 5, 2012
Study Record Updates
Last Update Posted (Estimate)
March 6, 2012
Last Update Submitted That Met QC Criteria
March 4, 2012
Last Verified
December 1, 2011
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- NCT00289921
- 029399 (Other Identifier: EU)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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