Clinical Trials Logo

Clinical Trial Summary

The aim of present study is to evaluate whether a program of behavioral and cognitive procedures for emotional control, and assertive training, produces well-being and improvement in quality of life of healthy volunteers.


Clinical Trial Description

Healthy volunteers,not presenting neurologic or psychiatric disorders, 18 years or older,both genders, were selected, after a medical examination, to participate in the study. In a randomized controlled trial, the volunteers were submitted to sessions of muscle relaxation (autogenic method), progressive self-focus meditation, and cognitive-behavioral training in self-control of negatives feelings. They were also trained to determine goals and to determine each step to reach them (plan of action).The volunteers have to apply this strategy to control emotional behavior and improve interpersonal relationship. Anxiety and depression scores will be determined using the Beck self evaluation scales (BDI and BAI); quality of life will be determined using WHO-QOL inventory and the Ryff Scale will be used to measure Psychological Well-Being. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor)


Related Conditions & MeSH terms


NCT number NCT01823601
Study type Interventional
Source Centro de Estudos em Medicina Comportamental
Contact
Status Completed
Phase N/A
Start date January 2013
Completion date March 2013

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT05844878 - Dental Anxiety Management by Behavioral Therapeutic Techniques Among Iraqi Adult Patients Seeking Private Dental Care N/A