Psychosocial Factors a Prognostic Study of Pain in Patients With CMC Osteoarthritis
Status unconfirmed · Not applicable
Conditions studied: Pain, Osteoarthritis
In brief
In this clinical trial, females with a diagnosis of thumb CMC OA, will be recruited. The primary outcome of potential risk factors of osteoarthritis, pain and function will be measured using the demographic data, visual analog scale (VAS) and Disabilities of the Arm, Shoulder and Hand (QuickDASH). Secondary out-comes will include the Pain Self-Efficacy Questionnaire (PSEQ), Tampa Scale of Kinesiophobia (TSK), Fear Avoidance Beliefs Questionnaire (FABQ), Hospital Anxiety and Depression Scale (HADS) and Impairment and Functioning Inventory (IFI). Measurements will be taken at the baseline, three, six and 12 months follow up.
Key facts
- Study ID
- NCT03821298
- Run by
- Gannon University
- People needed
- 50
- Starts
- 2019-04-01
- Expected to finish
- 2020-04-01
- Last updated by the study team
- 2019-07-31
Who can join
Age: 18 and older, up to 90. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- women older than 18 years
- diagnosed with bilateral thumb CMC OA
- a reported pain intensity during activities of daily living (ADLs) of up to 4 of 10 on the visual analog scale (VAS)
- The referring hand surgeon will made the diagnosis of CMC OA based on radiographs and clinical exploration.
You may not qualify if…
- neurologic disorder affecting the upper limb
- had received previous treatment for their hand problem in the last 6 months including an intra-articular joint injection to wrist, fingers, or thumb
- had fractures or a significant hand injury or previous surgery to the wrist or hand
- had hand or finger tenosynovitis and/or Dupuytren disease
- patients who did not complete any questionnaire or if they did not sign the informed consent.
Where it is running
- Gannon University — Ruskin, Florida, United States (enrolling)
Full record on ClinicalTrials.gov
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