Anxiety Clinical Trial
Official title:
Use of Massage Therapy to Reduce Anxiety and Improve Sleep in Patients Participating in an Inpatient Withdrawal Management (Detox) Program: A Randomized Controlled Pilot Study
Verified date | January 2009 |
Source | Dalhousie University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Ethics Review Committee |
Study type | Interventional |
In Canada, Addiction Prevention and Treatment Service's (APTS) offer programs specifically
designed to help people withdrawal from psychoactive drugs. While participants of withdrawal
management (Detox) programs generally reach their goals, the process is a difficult one
often exacting an emotional and physical toll. Troublesome symptoms of withdrawal from
psychoactive drugs may include anxiety and sleep disturbances. If untreated these symptoms
can lead to discontinuation of withdrawal and /or affect the introduction of
cognitive-behavioral and or motivational therapy components of Detox programs. In Detox the
symptoms of withdraw are managed pharmacologically. Pharmacological tools for managing
anxiety and sleep disturbances exist and while effective and safe, in many clinical
settings, have limitations and liability in the addiction treatment setting. To address
these concerns APTS has incorporated non-pharmacological anxiety management practices into
its programs. Prominent among these is therapeutic massage (chair massage in the Swedish
tradition). While therapeutic massage has been shown to reduce state and trait anxiety in a
variety of clinical settings, no previous study has assessed its anxiolytic or sleep
promoting efficacy in an addiction treatment setting. In keeping with ATPS's policy on
evidence-based practice, evidence in support of this practice is now required.
Research Objectives: We propose to test the Hypothesis: Therapeutic Massage is an effective
therapy for managing withdrawal-related anxiety and for improving sleep effectiveness in
patients withdrawing from psychoactive drugs. Our specific objective is to perform a
randomized controlled trial (RCT) to determine whether therapeutic massage is effective in
comparison to relaxation control treatment in reducing the levels of state and trait anxiety
associated with withdrawal and in promoting sleep efficiency.
Research Design: A RCT of the effects of therapeutic massage will be conducted on 80
patients (ages 18-65) attending an APTS Detox program. Patients will be assigned to 1 of 2
treatment groups (n=40/group) and will receive either: therapeutic massage or relaxation
control treatment once a day for 3 consecutive days. Anxiety, state and trait, will be
measured pre and post each treatment through a standardized tool and physiologic measures
(heart rate & blood pre(state and trait) and sleep efficiency will be determined through
actigraphy and daily sleep logs.
Status | Completed |
Enrollment | 80 |
Est. completion date | January 2009 |
Est. primary completion date | January 2009 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Individuals receiving inpatient treatment for withdrawal from psychoactive drugs and who were able to give informed consent and comply with study procedures were eligible to participate. - being at least 18 years of age; - self-reported primary presenting problem as one of the following: alcohol, cocaine, or opioids Exclusion Criteria: - prior treatment or experience with massage therapy - prior history of anxiety or sleep disorder - history of coagulation or platelet disorders or be currently taking medications that may promote bleeding - contraindications to the treatment intervention as described in the standards of care of the College of Massage Therapists of Ontario (http://www.cmto.com/regulations/standard.htm). |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Canada | Addiction Prevention and Treatment Services; Capital District | Halifax | Nova Scotia |
Lead Sponsor | Collaborator |
---|---|
Dalhousie University | Holistic Health Research Foundation of Canada |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | State and Trait Anxiety (Spielberger State Trait Anxiety Inventory of Adults (Y1 and Y2)) | State and trait anxiety scores will be determined at baseline (at the time of recruitment into the study) and then immediately prior to and within 10 minutes following each intervention session (pre/post design) | No | |
Secondary | Heart Rate and Blood Pressure | Heart rate and blood pressure will be measured at baseline (at the time of recruitment into the study) and then immediately prior to and within 10 minutes following each intervention session (pre/post design) | No | |
Secondary | Sleep Quality | On each intervention day subjects will wear an actigraph during normal sleep time. They will also be asked to complete a sleep log in the morning, upon waking for each post-intervention day | No |
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