Evaluation of Quality of Life in Women
Investigation of Affecting Factors Quality of Life in Women
1 other identifier
interventional
227
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable quality-of-life
Started Nov 2019
Shorter than P25 for not_applicable quality-of-life
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 13, 2019
CompletedFirst Posted
Study publicly available on registry
November 15, 2019
CompletedStudy Start
First participant enrolled
November 30, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
June 28, 2020
CompletedJune 30, 2020
June 1, 2020
6 months
November 13, 2019
June 29, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
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 Outcomes (4)
Social Functioning Scale
10 minutes
Depression scale
5 minutes
physical activity level
5 minutes
Musculoskeletal status
5 minutes
Study Arms (1)
Experimental Group: quality of life assessment
EXPERIMENTALWomen's quality of life will be evaluated.
Interventions
Quality of life will be assessed with Nottingham Health Profile
Eligibility Criteria
You may qualify if:
- To be a volunteer
You may not qualify if:
- having severe musculoskeletal system disorders
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hacettepe University
Ankara, 06100, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PT, Research Assisstant, MSc
Study Record Dates
First Submitted
November 13, 2019
First Posted
November 15, 2019
Study Start
November 30, 2019
Primary Completion
June 1, 2020
Study Completion
June 28, 2020
Last Updated
June 30, 2020
Record last verified: 2020-06
Data Sharing
- IPD Sharing
- Will not share