Generalized Anxiety Disorder Clinical Trial
Official title:
Efficacy of Massage and Light Touch Therapy for the Treatment of Generalized Anxiety Disorder
There is an impressive and growing body of data suggesting that massage therapy is effective
in decreasing some symptoms of pathological conditions as well as facilitating growth,
reducing pain, increasing alertness, diminishing symptoms of depression and anxiety, and
enhancing immune function. Preliminary studies suggest that massage therapy decreases
symptoms of anxiety and depression, and lowers salivary cortisol levels in a wide array of
childhood and adult neuropsychiatric disorders including post-traumatic stress disorder,
attention-deficit-disorder hyperactivity, depression, bulimia and anorexia-nervosa.
Generalized Anxiety Disorder (GAD) is characterized by the presence of a constellation of
signs and symptoms for at least 6 months in duration, with some type of functional disability
or decrease in quality of life. The signs and symptoms of GAD include a myriad of somatic
symptoms including muscle tension, headaches, backaches, fatigue, restlessness, insomnia, as
well as psychological feelings of worry, anxiety, and feeling overwhelmed. Both
pharmacotherapy and psychotherapy are effective in decreasing the signs and symptoms of GAD.
Unfortunately, the vast majority of patients with GAD never receive adequate pharmacotherapy
or psychotherapy. Therefore, the development of a complementary and alternative therapy that
has demonstrated efficacy for GAD might be well received by patients.
This study's goals are to investigate the efficacy of Swedish massage therapy vs. light touch
therapy and better understand the biological effects of massage in patients with anxiety.
Qualified participants will be randomly assigned to one of two groups in which they will
receive Swedish massage therapy twice per week for 12 weeks or Light Touch therapy twice per
week for 6 weeks followed by Swedish massage therapy twice per week for the next 6 weeks. The
total length of the study is 13 weeks, which includes a screening visit that takes about 3
hours and two therapy visits per week for 12 weeks that last about 1 hour each. Blood and
urine will be collected at three of the visits. Compensation is up to $400 for completing the
entire study.
n/a
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
NCT03420456 -
Transcranial Pulse Near-Infrared Light in Generalized Anxiety Disorder: a Placebo-Controlled Study
|
N/A | |
Active, not recruiting |
NCT05530642 -
An Augmented Training Program for Preventing Post-Traumatic Stress Injuries Among Diverse Public Safety Personnel
|
N/A | |
Withdrawn |
NCT02382224 -
Worry Exposure for Generalized Anxiety Disorder
|
N/A | |
Completed |
NCT02256566 -
Cognitive Training for Mood and Anxiety Disorders
|
N/A | |
Completed |
NCT02306356 -
Internet-delivered Treatment for Children With Anxiety Disorders in a Rural Area; an Open Trial in a Clinical Setting
|
N/A | |
Completed |
NCT01958788 -
Testing Beliefs About Uncertainty in the Treatment of Generalized Anxiety Disorder
|
N/A | |
Completed |
NCT01681329 -
Cognitive-Behavioral Treatment and Interpretation Modification Training for Adults With Generalized Anxiety Disorder
|
N/A | |
Completed |
NCT01201967 -
A Collaborative Care Program to Improve Treatment of Depression and Anxiety Disorders in Cardiac Patients
|
Phase 4 | |
Completed |
NCT01342120 -
PHARMO Institute Seroquel Safety Study
|
N/A | |
Completed |
NCT01203293 -
Cognitive Behavioral Therapy (CBT) for Latinos With Generalized Anxiety Disorder in the General Medical Sector
|
Phase 1 | |
Completed |
NCT00961298 -
An Open Label Trial of Duloxetine in the Treatment of Irritable Bowel Syndrome and Comorbid Generalized Anxiety Disorder
|
Phase 4 | |
Completed |
NCT01971203 -
Efficacy of Extended-release Quetiapine (Seroquel XR) as Adjunctive Therapy to Cognitive Behavioral Therapy in the Treat
|
N/A | |
Terminated |
NCT01244711 -
Open-Label Pilot Study to Examine the Value of Substituting Quetiapine for Benzodiazepines
|
Phase 4 | |
Completed |
NCT00744627 -
Efficacy and Safety of Vortioxetine (Lu AA21004) for Treatment of Generalized Anxiety Disorder in Adults.
|
Phase 3 | |
Completed |
NCT00711737 -
Study of the Changes in Metabolic Parameters in Patients Treated With Escitalopram for Six Months
|
N/A | |
Completed |
NCT00515242 -
Therapeutic Massage for Generalized Anxiety Disorder
|
Phase 1/Phase 2 | |
Completed |
NCT00537615 -
An Open-label Study to Investigate the Absorption, Metabolism and Excretion of Radiolabeled PD 0332334 in Six Healthy Male Volunteers
|
Phase 1 | |
Completed |
NCT00525226 -
Evaluating the Effects of Stress in Pregnancy
|
N/A | |
Completed |
NCT00620776 -
Combined Treatment for Generalized Anxiety Disorder (GAD)
|
Phase 2 | |
Completed |
NCT00368745 -
Efficacy and Safety of Pregabalin vs Placebo for Generalized Anxiety Disorder (GAD) Symptoms in Subjects Discontinuing Benzodiazepine Treatment and Remaining 6 Weeks on Study Medication, Free From Benzodiazepine Use.
|
Phase 3 |