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Participation in Occupations and Perception of Quality of Life, Comparing Adults With and Without PTSD

Z

Ziv Hospital

Status

Unknown

Conditions

Post Traumatic Stress Disorder

Study type

Observational

Funder types

Other

Identifiers

NCT03350438
0023-17-ziv

Details and patient eligibility

About

This study assesses the relationship between participation and quality of life the way adults with and without Post Traumatic Stress Disorder (PTSD) experience it in everyday life. Both groups will fill out Questionnaires and the answers will be compared. In addition different aspects of dissociation will be taken in to consideration.

Full description

Post Traumatic Stress Disorder has been known to severely impair participation in everyday activities such as work, recreation and social participation. In turn, these impairments can diminish quality of life. However, the relationship between PTSD, functioning and quality of life remains incompletely understood.

Since achieving full participation in daily activities is the main goal of occupational therapy, and since quality of life is a primary treatment success measure, it is important to fully understand the relationship between PTSD, participation and quality of life.

Various studies show that dissociation affects different body functions that manage and monitor mental functioning. Since quality of life is a subjective measure that relies on one's ability to mentally represent himself and others it is important to tack into consideration the way that dissociation affects the relationships described above.

The research contains 4 Questionnaires that will be filed out by the participants and the data from the Questionnaires will be analyzed and compared.

Enrollment

80 estimated patients

Sex

Male

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hebrew speaking, read and write in Hebrew, have been diagnosed with PTSD following a trauma that occurred over one year before the current study.

Exclusion criteria

  • Other psychiatric disorders, cognitive or physical impairments.

Trial design

80 participants in 2 patient groups

PTSD Patients
Description:
patients ranging 18-60, diagnosed with PTSD following a trauma that occured over one year before the current study and do not have other health problems that may affect their everyday participation.
healthy adults
Description:
healthy adults, ranging 18-60, without any health problems that may affect their everyday participation.

Trial contacts and locations

1

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Central trial contact

ariela rosenblum, BA

Data sourced from clinicaltrials.gov

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