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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04164628
Other study ID # GO 19/1046
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 30, 2019
Est. completion date June 28, 2020

Study information

Verified date June 2020
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

300 women will be evaluated in this study. Their quality of life, level of physical activity, Social Functioning, levels of depression and musculoskeletal status will be assessed.


Description:

Many factors affects quality of life in women. In the literature, factors affecting the quality of life such as diseases, working conditions and psychological factors of women have been investigated in different diseases. However, there was no study investigating the factors affecting quality of life for a sample of adult female individuals. Therefore, the aim of our study is to investigate the effect of social, psychological and physical variables that we think may affect the quality of life in women.


Recruitment information / eligibility

Status Completed
Enrollment 227
Est. completion date June 28, 2020
Est. primary completion date June 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- To be a volunteer

Exclusion Criteria:

- having severe musculoskeletal system disorders

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Quality of life assessment
Quality of life will be assessed with Nottingham Health Profile

Locations

Country Name City State
Turkey Hacettepe University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of life The Nottingham Health Profile is a general patient self-evaluation of subjective health status. The score of this questionnaire ranges between 0 and 600. The higher score indicates the worse quality of life. 5 minutes
Secondary Social Functioning Scale Questionnaire is specifically designed to assess the most relevant areas of social functioning. The higher score indicates the better social function. 10 minutes
Secondary Depression scale The Beck Depression Inventory is a 21-item self-administered scale measuring various symptoms of depression. It comprises 21 groups of statements describing the somatic and cognitive-emotional symptoms of depression. Each item consists of four alternative responses.
graded from 0 to 3 according to the severity of the symptom. The patients choose the response closest to their state during the past week. A sum score is counted, a higher score indicating more severe depression
5 minutes
Secondary physical activity level Physical activity was assessed using the self-administered short (7-item) forms of the international physical activity questionnaire. The higher score indicates the more physically active lifestyle. 5 minutes
Secondary Musculoskeletal status The Nordic musculoskeletal questionnaire includes 27 items exploring the presence of musculoskeletal symptoms during a 12-month period covering the nine different parts of the body. The higher score indicates the worse musculoskeletal status. 5 minutes
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