Investigation of Pain Coping Methods and Related Factors in Postmenopausal Women
1 other identifier
observational
60
1 country
1
Brief Summary
Musculoskeletal pain (MSP) reflects of musculoskeletal conditions related to tissues such as tendons, muscles, ligaments, nerves, and other joint structures. Coping strategies with pain are used to manage the pain and its impacts. The present study aimed to compare active and passive coping strategies used and pain severity in postmenopausal women according to their demographic characteristics. Also, the relationship between pain and coping strategies in postmenopausal women with cMSP will be examined.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Sep 2020
Shorter than P25 for all trials
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
September 2, 2020
CompletedFirst Posted
Study publicly available on registry
September 10, 2020
CompletedStudy Start
First participant enrolled
September 17, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 30, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
November 15, 2020
CompletedJanuary 8, 2021
January 1, 2021
1 month
September 2, 2020
January 7, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
McGill Pain Questionnaire
This tool is used for assesment of pain, namely; body part of pain, timeframe, characteristic and severity of pain. As score increases, pain condition worsens.
15 minutes
Pain Coping Inventory (PCI)
This tool is used for assessment of pain coping strategies. The higher score received means that coping strategy is used more.
10 minutes
Timed up and go test
This tool is used for assessment of functional mobility. The duration to complete the task (in seconds) is used as a score. As the score increase, the functional mobility decrease.
5 minutes
Eligibility Criteria
Patients presented to a rehabilitation clinic with complaints of pain in anywhere of their body and who are volunteer for the study will be included. Informed consent will be signed by the participants.
You may qualify if:
- complaints of pain in anywhere of their body.
- presenting at least 1 year of amenorrhea
- being between the ages of 50-69 years.
You may not qualify if:
- have rheumatological, orthopedic and neurological diseases,
- have compression fractures, malignancies,
- have a chronic disease that will lead to secondary osteoporosis,
- have a drug use that will lead to secondary osteoporosis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
European University of Lefke
Mersin, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Beliz B Kaygısız, PT, PhD
European University of Lefke
- STUDY DIRECTOR
Nuray Elibol
Ege University
- STUDY CHAIR
Sevim Acaröz Candan
Ordu University
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 2, 2020
First Posted
September 10, 2020
Study Start
September 17, 2020
Primary Completion
October 30, 2020
Study Completion
November 15, 2020
Last Updated
January 8, 2021
Record last verified: 2021-01