Ignite Creation Date:
2024-05-05 @ 11:23 AM
Last Modification Date:
2024-10-26 @ 9:06 AM
Study NCT ID:
NCT00010621
Status:
COMPLETED
Last Update Posted:
2006-08-18
First Post:
2001-02-02
Brief Title:
Complementary Medicine Approaches to TMD Pain Management
Sponsor:
National Center for Complementary and Integrative Health NCCIH
Organization:
National Center for Complementary and Integrative Health NCCIH
Study Overview
Official Title:
Complementary Medicine Approaches to TMD Pain Management
Status:
COMPLETED
Status Verified Date:
2006-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study will determine whether selected complementary approaches to temporomandibular joint TMJ pain management-acupuncture are as effective as usual care
Detailed Description:
Temporomandibular disorders are characterized by pain and tenderness in the muscles of mastication andor the TMJ limitations of jaw opening often accompanied by deviations in mandibular path and clicking popping or grating TMJ sounds This study will compare the effectiveness of the complementary therapies chiropractic therapy and bodywork therapy to the standard of care for TMJ pain If these complementary interventions are shown to be effective the goal is to design and implement a Phase III clinical trial to further evaluate the health consequences and cost of these therapies
Participants will be evaluated at baseline and 6 and 12 months post-intervention Clinical examinations saliva samples to assess salivary cortisol levels and a series of questionnaires to assess pain and grade of dysfunctional pain psychological functioning and other physical symptoms will be used to assess outcomes The investigators will passively monitor health care utilization within KPNW using clinical research and administrative databases
Participants will be evaluated at baseline and 6 and 12 months post-intervention Clinical examinations saliva samples to assess salivary cortisol levels and a series of questionnaires to assess pain and grade of dysfunctional pain psychological functioning and other physical symptoms will be used to assess outcomes The investigators will passively monitor health care utilization within KPNW using clinical research and administrative databases
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| P50AT000076-01 | NIH | None | httpsreporternihgovquickSearchP50AT000076-01 |