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DeQuervain's tenosynovitis is characterized by pain on the pain on the radial (thumb) side of the wrist problems with thumb function. At this point, the standard care is to change daily activities, use a thumb brace, and the possible use of painkillers. There is a difference in opinion among physical therapists about how to use the splint in the treatment of DeQuervain tenosynovitis. Some physicians tell patients to wear the brace at all times while other therapists encourage patients to exercise and use the brace as needed. Both approaches to using the splint are accepted as standard. The purpose of this study is to test and evaluate these two ways of splinting and assess which one is better for patients with DeQuervain tenosynovitis.
De Quervain's tenosynovitis (stenosing tenosynovitis of the first dorsal extensor compartment) is characterized by pain on the radial (thumb) side of the wrist and impairment of thumb and wrist function. Histological evaluation is consistent with a chronic rather than an acute tenosynovitis consistent with the often prolonged course of this disease.
Nonoperative treatments include modification of activities, splint immobilization, icing and anti-inflammatory medication, and corticosteroid injections. Long opponens splinting (or short arm thumb spica splinting; a splint that immobilizes the wrist and the thumb) is standard and well accepted. There is no consensus on the best protocol for use of the splint. Some authors advocate full time splinting for 4 - 6 weeks, with the rationale that tendonitis will resolve with strict rest. Other authors, perhaps aware of histological evidence that De quervain's is a chronic rather than acute inflammatory condition, feel that the splint serves merely to relieve symptoms and is best used as best suits each individual patient. To our knowledge, there are not data available regarding these disparate views.
The ultimate prognosis for recovery in the condition seems satisfying, regardless of the treatment, and spontaneous recovery is the rule. Psychological and personality factors, such as pain anxiety, catastrophizing, and depression are strongly related to upper extremity specific health status and may also influence recovery.
The primary goal of this study is to determine which protocol of splinting leads to better outcome in non-surgical treatment of DeQuervain's tenosynovitis. As a secondary goal and to generate hypotheses for later studies we would like to evaluate the influence of psychosocial factors on both objective (grip strength) and subjective (DASH questionnaire) measures of outcome.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Subjects who wear the splint whenever the feel the need. | ||
| 2 | Subjects who wear the splint whenever possible. |
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| Measure | Description | Time Frame |
|---|---|---|
| Disabilities of the Arm, Shoulder, and Hand (DASH) Questionnaire | The DASH questionnaire measures upper extremity disability on a scale from 0-100, where 0 is no disability and 100 is severe disability. | 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Grip Strength | Grip strength is measured as a percentage of the non-affected or least affected side. | 8 weeks |
| Treatment Satisfaction | Treatment satisfaction was measured on a scale from 0-10, where 0 is complete dissatisfaction and 10 is complete satisfaction |
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Inclusion Criteria:
Exclusion Criteria:
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Patients from the MGH Hand and Upper Extremity Service.
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| Name | Affiliation | Role |
|---|---|---|
| David Ring, MD, PhD | Massachusetts General Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | As-Desired Splinting | Subjects who wear the splint as desired |
| FG001 | Full Time Splinting | Subjects who wear the splint as much as possible |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | As-Desired Splinting | Subjects who wear the splint as desired |
| BG001 | Full Time Splinting | Subjects who wear the splint as much as possible |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Disabilities of the Arm, Shoulder, and Hand (DASH) Questionnaire | The DASH questionnaire measures upper extremity disability on a scale from 0-100, where 0 is no disability and 100 is severe disability. | Posted | Mean | Standard Deviation | units on a scale | 8 weeks |
|
|
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | As-Desired Splinting | Subjects who wear the splint as desired | 0 |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Taylor Pong | Massachusetts General Hospital | tpong1@partners.org |
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| ID | Term |
|---|---|
| D010549 | Personal Satisfaction |
| ID | Term |
|---|---|
| D001519 | Behavior |
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| 8 weeks |
| Pain Intensity | Pain intensity was measured using the Numeric Rating Scale, on a scale from 0-10, where 0 is no pain and 10 is the most pain. | 8 weeks |
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaire | The DASH questionnaire measures the upper extremity disability on a scale from 0-100, 0 is no disability and 100 is the most disability. | Mean | Standard Deviation | units on a scale |
|
| Pain Intensity | Pain intensity was measured using the Numeric Rating Scale, on a scale from 0-10, where 0 is no pain and 10 is the most pain. | Mean | Standard Deviation | units on a scale |
|
| Center for Epidemiologic Studies Depression Scale - Revised (CES-D) | The CESD-R measures symptom of depression in nine different groups. The range of possible scores is between 0 (for those who say 'not at all or less than one day to all 20 questions) and 60 (nearly everyday for 2 weeks for all 20 questions). | Mean | Standard Deviation | units on a scale |
|
| Pain Catastrophizing scale (PCS) | The Pain Catastrophizing Scale measures a set of mal-adaptive cognitive conditions while in pain. The score ranges from 0-52, ranging from least to most catastrophic thinking. | Mean | Standard Deviation | units on a scale |
|
| Grip Strength | Grip strength measured as a percentage of the non-affected hand. | Mean | Standard Deviation | percentage of non-affected hand |
|
| Counts |
|---|
| Participants |
|
|
| Secondary | Grip Strength | Grip strength is measured as a percentage of the non-affected or least affected side. | Posted | Mean | Standard Deviation | percentage of non-affected hand | 8 weeks |
|
|
|
| Secondary | Treatment Satisfaction | Treatment satisfaction was measured on a scale from 0-10, where 0 is complete dissatisfaction and 10 is complete satisfaction | Posted | Mean | Standard Deviation | units on a scale | 8 weeks |
|
|
|
| Secondary | Pain Intensity | Pain intensity was measured using the Numeric Rating Scale, on a scale from 0-10, where 0 is no pain and 10 is the most pain. | Posted | Mean | Standard Deviation | units on a scale | 8 weeks |
|
|
|
| 43 |
| 0 |
| 43 |
| 0 |
| 43 |
| EG001 | Full Time Splinting | Subjects who wear the splint as much as possible | 0 | 40 | 0 | 40 | 0 | 40 |
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