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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01253486
Other study ID # GMM 2010
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2010
Est. completion date May 2013

Study information

Verified date February 2021
Source Istituto Auxologico Italiano
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will determine whether the psychological and physical benefits of expressive writing extend to obese in-patients with Ischemic Heart Disease (IHD)referred to cardiac rehabilitation


Description:

Expressive writing, for as little as 3-5 sessions of 20 minutes, has been found to improve both physical and psychological health based on health outcome measures such as number of doctor's visits and hospital days, blood pressure control, lung and immune function, pain, anxiety and depression. Given its simplicity and obvious advantages in terms of cost-effectiveness, expressive writing has great potential as a therapeutic tool or as a means of self-help, either alone or as an adjunct to traditional therapies. This modality has not been studied in obese patients with Ischemic Heart Disease.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date May 2013
Est. primary completion date September 2012
Accepts healthy volunteers No
Gender All
Age group N/A to 70 Years
Eligibility Inclusion Criteria: - obesity - Ischemic Heart disease - Signed informed consent Exclusion Criteria: - Visual or manual limitations that preclude reading and writing - Unwilling to participate

Study Design


Intervention

Behavioral:
Disease-related Expressive writing
Participants in the disease-related expressive writing condition write about their feelings about cardiac disease four times, for at least 20 minutes each time, during a two week period.
Active Comparator: Traditional expressive writing
Participants in the traditional expressive writing condition write about their feelings about one or more stressful experiences they lived in the past, for at least 20 minutes each time, during a two week period
Sham Comparator: Neutral writing
Participants in the neutral writing condition write about the facts about cardiac disease, for at least 20 minutes each time, during a two week period

Locations

Country Name City State
Italy San Giuseppe Hospital, Istituto Auxologico Italiano IRCSS Verbania

Sponsors (1)

Lead Sponsor Collaborator
Istituto Auxologico Italiano

Country where clinical trial is conducted

Italy, 

References & Publications (1)

Frattaroli J. Experimental disclosure and its moderators: a meta-analysis. Psychol Bull. 2006 Nov;132(6):823-65. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary SF12 The SF12 is a generic measure of both physical and emotional components of health-related quality of life 1 year
Primary BDI-II The Beck Depression Inventory is a measure of depressive symptoms 1 year
Primary BDI The Beck Anxiety Inventory is a measure of cognitive and somatic symptoms of anxiety 1 year
Primary Brief-PTGI The Brief Post-Traumatic Growth Inventory is a measure of positive growth following adversity 1 year
Secondary BMI Body Mass Index (BMI) is a measure of obesity and is calculated as weight in kilograms divided by height in meters squared 1 year
Secondary Multiple Coronary Risk Factors Hypertension, HDL, LDL, 1 year
Secondary METs Metabolic equivalents are a measure of exercise capacity. 1 MET represents the amount of oxygen consumed at rest and is equal to approximately 3.5 ml O2 kg-1 min-1 1 year
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