Heart Failure. Chronic Systolic (Congestive) Heart Failure
Conditions
Interventions
Intervention 1: Control Group Did not Receive Behavioral Intervention and Receive only Treatment Routine Care. Intervention 2: Type of Intervention Is Behavioral, In addition to routine medical cares,
whereas, their negative behaviors will be undermined by mentioning their complications and disadvantages. The intervention group will also receive telephone and physically individual consultation. The
Behavior
Control Group Did not Receive Behavioral Intervention and Receive only Treatment Routine Care.
Type of Intervention Is Behavioral, In addition to routine medical cares, the intervention group will receive weekly 45-minute sessions of Roy's Adaptation Model-based training for one month. This gro
Sponsors
Ahvaze University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria are: diagnosis of class I, II, III heart failure by a physician, according to the American Heart Association and clinical and laboratory evidence, at least 6 months before the study; ejection fraction of 40% or below; no mental disorder; normal hearing, vision and mental capabilities that allow making communication; age range from 18 to 65 years; no contraction of other chronic diseases such as kidney or liver failure, chronic pulmonary obstructive diseases, and neural and motor disorders, except diabetes; having access to patients for follow-up controls; walking capability; and not receiving the same training in other centers. Exclusion criteria include: unwillingness to participate for any reason; moving from the research region during the study; and more than two times absence from training sessions.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of Life. Timepoint: Before Intervention and one Month After Intervention. Method of measurement: Minnesota Questionnaire, Roy Questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Adaptation. Timepoint: before itervention and one month after intervention. Method of measurement: Roy Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDoctor Shahram Baraz
Ahvaz University of Medical Sciences
Outcome results
None listed