Quality of Life Clinical Trial
— NADAOfficial title:
"Auricular Acupuncture and Cognitive Behavioral Therapy in the Context of Insomnia and Low Dose Dependence of Benzodiazepine-like Drugs and Other Sleep Medicine With Addiction Risk"
| Verified date | May 2015 |
| Source | Uppsala University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Sweden: Institutional Review Board |
| Study type | Interventional |
"Auricular acupuncture and cognitive behavioral therapy in the context of insomnia and low
dose dependence of benzodiazepine-like drugs and other sleep medicine with addiction risk"
INTRODUCTION: Insomnia is a common health problem in Sweden, which increases with age and is
more prevalent among women.
It is defined by unsatisfied sleep quality during more than a month's time. The main
symptoms are difficulties falling- and/or maintaining sleep, involuntary awakenings during
the night of early morning, day time sleepiness and decreased will for day time activity due
to sleepiness. Insomnia is ranked to be the fifth most common cause of prescription of
medicine at the outpatient clinics in general health care in Sweden. In 2008 a prevalence
study was initiated in Sweden by the Swedish Council on Health Technology Assessment (SBU).
The study showed that 24% of the Swedish population suffered from sleep disorders. Sleeping
disorders can go on for many years and can therefore entail significant personal suffering.
Usually sleep medicine combined with general sleeping advices is the first-hand treatment
for insomnia. However, according to SBU, first treatment should be non-pharmacological, for
instance cognitive behavioral therapy (CBT). Despite this recommendation the prescribing of
sleep medicine is still high.
There are studies that suggest auricular acupuncture (AA) to be an effective method to treat
insomnia. However more evidence is needed to draw firm conclusions.
AIM: The aim of the study is to investigate if AA is as effective as CBT to treat insomnia
for patients who have stopped using benzodiazepine-like sleep medicine.
METHOD: This is a randomized controlled study (RTC) including patients suffering from
insomnia, with a low dose dependence of benzodiazepine-like drugs. The patients will be
recruited from primary care and from an out-patient clinic specialized in sleeping disorders
and also by add in the local news paper. The respondents will be randomized to one of two
groups; group I will receive AA twice a week for 4 weeks; group II will receive CBT once a
week for six weeks. After three months there will be a long-time follow up in order to
investigate a potential long-term effect.
| Status | Completed |
| Enrollment | 60 |
| Est. completion date | May 2015 |
| Est. primary completion date | April 2015 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 18 Years to 75 Years |
| Eligibility |
Inclusion Criteria: - men and women (n=40) - 18-75 years old with: (i) primary or secondary insomnia who have been treated every day for over six months with benzodiazepine-like drugs and developed a low dose drug dependence, and (ii) people suffering from insomnia who use benzodiazepine-like drugs = three nights a week with no effect. Exclusion Criteria: - high dose drug dependence, - generalized anxiety disorder (GAD), - patients diagnosed with diagnosed psychotic disorders, - personality disorders or serious somatic illness, - alcohol dependence/abuse, - anti psychotic medications, - pain reliving treatment with methadone- or methadone like drugs, - new onset depression, - patients who have initiated or changed their anti-depressant,anxiolytic or pregabalin medication during the last six months, - pregnancy. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Sweden | Uppsala University Hospital | Uppsala |
| Lead Sponsor | Collaborator |
|---|---|
| Uppsala University |
Sweden,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Insomnia | Outcome will be measured by: i)actigraphy ii)evaluated questionary forms: Insomnia Severity Index (ISI) Hospital Anxiety Depression scale (HAD) Minimal Insomnia Symptom Scale (MISS) Ep-worth Sleepless scale (ESS) Dysfunctional Belief About Sleep (DBAS-16) Functional Outcome of Sleep Questionaire (FOSQ) |
five months | No |
| Secondary | Quality of life | Quality of life will be measured by using "Form SF-12". | five months | No |
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