Opiate Craving Reduction Study Using Post-detox Patients on Suboxone and Use of TEAS as Adjunctive Treatment
Status: | Withdrawn |
---|---|
Healthy: | No |
Age Range: | 18 - 59 |
Updated: | 2/23/2018 |
Start Date: | August 2015 |
End Date: | December 2017 |
A Crossover Study Using Transdermal Electroacupuncture as Adjunctive Treatment to Reduce Opiate Cravings in Post-Detox Outpatients Receiving Buprenorphine-Naloxone
Pilot study of 12 outpatients in early recovery from illicit drug use,post-detox and on
buprenorphine-naloxone maintenance will be offered 12 TEAS adjunct treatments over 6
weeks(X2/week) to ascertain if they experience any improvement in mood,sleep,overall quality
of life and decrease drug cravings ultimately while facing everyday life stressors.
buprenorphine-naloxone maintenance will be offered 12 TEAS adjunct treatments over 6
weeks(X2/week) to ascertain if they experience any improvement in mood,sleep,overall quality
of life and decrease drug cravings ultimately while facing everyday life stressors.
- this crossover study will involve participants who will be randomized into two treatment
groups,A&B. TEAS treatments will be given for 30 minutes,X2/week,for 6 weeks(12total
sessions). Group A will receive 2 weeks(4 sessions) of active treatment followed by 4
weeks of sham treatment(8 sessions). Group B will receive 2 weeks(4 sessions) of sham
treatment,2 weeks (4 sessions)of real treatment,and finally 2 weeks (4 sessions) of sham
treatment.
- parameters to be measured include vital signs and questionnaires weeks 1,3,5,6 to assess
self-reported past 14-day substance use,alcohol and drug craving,withdrawal
symptoms,sleep,mood,pain and overall quality of life.
- goals include better lives for post-detox opiate addicts as they incorporate this
treatment into their lives,saving themselves and loved ones more horror,and their
communities resources.
groups,A&B. TEAS treatments will be given for 30 minutes,X2/week,for 6 weeks(12total
sessions). Group A will receive 2 weeks(4 sessions) of active treatment followed by 4
weeks of sham treatment(8 sessions). Group B will receive 2 weeks(4 sessions) of sham
treatment,2 weeks (4 sessions)of real treatment,and finally 2 weeks (4 sessions) of sham
treatment.
- parameters to be measured include vital signs and questionnaires weeks 1,3,5,6 to assess
self-reported past 14-day substance use,alcohol and drug craving,withdrawal
symptoms,sleep,mood,pain and overall quality of life.
- goals include better lives for post-detox opiate addicts as they incorporate this
treatment into their lives,saving themselves and loved ones more horror,and their
communities resources.
Inclusion Criteria:
- 18-59 years old
- early recovery(0-3months of abstinence
- not currently detoxing
- maintained on buprenorphine-naloxone under the care of qualified MD
- proficient in the English language
Exclusion Criteria:
- having acute,psychiatric symptoms which would pose safety concerns,or an adherence to
treatment barrier(active suicidality/psychosis/mania)
- severe cognitive disorders*not competent to give informed consent
- active cardiac disease or EKG abnormalities or with cardiac pacemaker
- currently detoxing from alcohol or illicit drugs
- inability or non-intention to attend all treatment sessions*history of
seizures*pregnancy or breast feeding.
We found this trial at
1
site
115 Mill St
Belmont, Massachusetts 02478
Belmont, Massachusetts 02478
(617) 855-2000
Principal Investigator: Barbara A MacIntyre, MSN, RN
McLean Hospital McLean Hospital is a comprehensive psychiatric hospital committed to providing easy access to...
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