- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05047380
The Relationship of Disability With Depression, Anxiety and Sleep Quality in Patients With Coccygodynia
Study Overview
Status
Conditions
Detailed Description
Coccygodynia often develops from an inappropriate sitting position or when standing up from a sitting position. In the advanced stages of coccygodynia the pain becomes continuous. Pain can be triggered by walking or standing for a long time. Patients may experience sacrococcygeal pain in the supine position and during sleep. It has been argued that the coexistence of coccygodynia and psychiatric disease is caused by the excessive activity of the pelvic region nerves. In addition, it has been stated that stress, depression and fear may lead to increased spasm in the pelvic floor muscles.It is stated in the literature that 62.9-75% of patients with chronic pain have at least one psychiatric disorder. The most common psychiatric comorbidities in patients with chronic pain are; major depression, somatoform disorders, and generalized anxiety disorder. The relationship between pain and psychological variables has been attributed to the fact that the sensorial pathways of pain and mood regulation are located in the same region of the brain. In addition, common neurotransmitters such as serotonin, norepinephrine and dopamine are present in the pathophysiology of depression and pain.There is a bidirectional relationship between sleep and pain. In recent studies; It has been reported that sleep disorder causes pain development rather than the effect of pain on sleep disorder.
54 patients with coccydynia will be recruited prospectively according to the appropriate inclusion and exclusion criteria.Within the scope of the study, the age, gender, duration of symptoms, etiology of coccygodynia, and severity of pain will be recorded. The Oswestry Disability Index scale will be filled in to assess the severity of disability resulting from pain in the patient. Pain severity will be evaluated with the Visual Analog Scale (VAS). Depression and anxiety assessment will be made with Beck Depression Scale and Beck Anxiety Scale, respectively. Sleep quality will be evaluated with the Pittsburg Sleep Quality Index.
The data will be entered into the SPSS (version: 22.0) IBM SPSS statistical package program. Arithmetic mean, standard deviation, min-max, median values will be given in the data obtained by measurement. Percentage and frequency distribution will be given in the data obtained by counting. In statistical evaluations, parametric tests will be used for normally distributed data, and non-parametric tests will be used for data not normally distributed. Relationships will be compared according to the Pearson or Spearman correlation coefficient. Chi-square test will be applied to categorical data. P<0.05 will be considered significant.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Hanzade A Ünal-Artık, MD
- Phone Number: +905057179039
- Email: hanzadeunal@windowslive.com
Study Locations
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Sivas, Turkey
- Recruiting
- Emel Guler
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Contact:
- emel guler
- Phone Number: +905356492951
- Email: emelguler@cumhuriyet.edu.tr
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Diagnosed with coccygodynia
- Agreement to take part in the study 18 to 70 years old
Exclusion Criteria:
- Presence of cognitive impairment that would limit answering the questions in the questionnaires
- History of psychotic disorder
- History of neurological disease (cerebrovascular accident, polyneuropathy, parkinson's, dementia, epilepsy),
- History of rheumatological disease, fibromyalgia and malignancy
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
coccycodinia group
A total of 54 patients diagnosed with coccycodinia
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All assessments will be made using questionairres.
The Oswestry Disability Index scale will be filled in to assess the severity of disability resulting from pain in the patient.
Pain severity will be evaluated with the Visual Analog Scale (VAS).
Depression and anxiety assessment will be made with Beck Depression Scale and Beck Anxiety Scale, respectively.
Sleep quality will be evaluated with the Pittsburg Sleep Quality Index.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anxiety and depression
Time Frame: The study will be completed in 9 months.
|
Beck Depression Scale will be used in depression interrogation.
≤9 points are classified as normal,10-16 points as mild depression,17-29 points as moderate depression, and 30-63 points as severe depression.Beck Anxiety Scale will be used in anxiety interrogation.
≤9 points are classified as normal, 10-18 points as mild anxiety, 19-29 points as moderate anxiety, and 30-63 points as severe anxiety.
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The study will be completed in 9 months.
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|
Sleep quality
Time Frame: The study will be completed in 9 months.
|
Sleep quality will be questioned with The Pittsburgh Sleep Quality Index.
Those who score ˃5 have poor sleep quality, and those who score ≤5 have "good sleep quality".
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The study will be completed in 9 months.
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Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021-06/20
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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