- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT04543435
Investigation of Pain Coping Methods and Related Factors in Postmenopausal Women
Studieoversikt
Status
Forhold
Detaljert beskrivelse
Musculoskeletal pain (MSP) reflects of musculoskeletal conditions related to tissues such as tendons, muscles, ligaments, nerves, and other joint structures. If MSP lasts for longer than three months, it becomes chronic. The prevalence of chronic MSP (cMSP) increases with aging and its ratio changes between 35,7% and 49,8%. The previous studies demonstrated the differences in the prevalence of cMSP between men and women. According to most of the studies, older women adults are more vulnerable to experience than men due to some differences in perception of pain such as biological characteristics, their roles in daily life, beliefs or coping strategies with pain.
Oestrogen has a prominent role in the physiology of muscles, tendons, ligaments, and bones. The decline of this sex hormone during menopause transition could lead to MSP, particularly in the postmenopausal period. Indeed, an increasing rate of cMSP in postmenopausal women has been reported.
Coping strategies with pain are used to manage the pain and its impacts. Coping with pain requires the self-regulation of individuals using cognitive and behavioral reactions. Dealing with cMSP is a process that can need the making of changes in daily life and activities This study aimed to compare active and passive coping strategies being used and pain severity in postmenopausal women according to their age, marital status, educational status, and exercise habits. Also, subdomains of strategies and subdomains of pain and the relationship between pain and coping strategies in postmenopausal women with cMSP will be examined.
Studietype
Registrering (Faktiske)
Kontakter og plasseringer
Studiesteder
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Mersin, Tyrkia
- European University of Lefke
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
Inclusion Criteria:
- complaints of pain in anywhere of their body.
- presenting at least 1 year of amenorrhea
- being between the ages of 50-69 years.
Exclusion Criteria:
- 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
Studieplan
Hvordan er studiet utformet?
Designdetaljer
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
McGill Pain Questionnaire
Tidsramme: 15 minutes
|
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)
Tidsramme: 10 minutes
|
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
Tidsramme: 5 minutes
|
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
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Beliz B Kaygısız, PT, PhD, European University of Lefke
- Studieleder: Nuray ELİBOL, Ege university
- Studiestol: Sevim Acaröz Candan, T.C. ORDU ÜNİVERSİTESİ
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- ÜEK/47/01/12/1920/05
Plan for individuelle deltakerdata (IPD)
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