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

NCT ID: NCT03350438

Last Updated: 2017-12-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-01-01

Study Completion Date

2018-10-30

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Post Traumatic Stress Disorder

Keywords

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participation quality of life occupational therapy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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PTSD Patients

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.

No interventions assigned to this group

healthy adults

healthy adults, ranging 18-60, without any health problems that may affect their everyday participation.

No interventions assigned to this group

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Ziv Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Lidia Isakson, PHD

Role: PRINCIPAL_INVESTIGATOR

Ziv Hospital

Locations

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Ziv Hospital

Safed, Galilee, Israel

Site Status

Countries

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Israel

Central Contacts

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ariela rosenblum, BA

Role: CONTACT

Phone: 0508434154

Email: [email protected]

Other Identifiers

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0023-17-ziv

Identifier Type: -

Identifier Source: org_study_id