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临床试验/NCT03171519
NCT03171519已完成不适用

Effects of Exercise and Acupuncture on Chronic Insomnia: a Randomized Control Trial

Universidade Federal de Goias1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2017年9月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
1
主要终点
Change from baseline anxiety to 12 weeks

研究概览

简要总结

Introduction: Chronic insomnia is a sleep disorder, characterized by difficulty in initiating and/or maintaining sleep, presence of non-restorative sleep, frequent awakenings or difficulty returning to sleep after each awakening, with a frequency of 3 nights/week, for at least 3 months. Pharmacologic therapy is the most commonly method used for its treatment, however, pharmacotherapy is associated with side effects. Thus, non-pharmacological therapies have been suggested as an alternative. Objective: To verify the effects of exercise associated with acupuncture on chronic insomnia. METHODS: 40 patients with chronic insomnia will be randomly assigned into two groups: CONTROL (n = 20) and ACUPUNCTURE (n = 20). The volunteers of the CONTROL group will be submitted to 12 weeks of aerobic exercise, performed on a treadmill, with frequency of 3 times / week and duration of 50 minutes / day. ACUPUNCTURE volunteers will perform aerobic exercise, following the protocol of the CONTROL group, plus acupuncture therapy once a week. The sleep evaluation will be evaluated by polysomnography and questionnaires. Expected Results: A 12-week combined therapy could potentiate the previously described positive effects of exercise in the treatment of chronic insomnia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
30 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •age 30-60 years;
  • •clinical diagnosis of chronic insomnia according to the DSM-V (performed by a physician specialized in Sleep Medicine);
  • •insomnia complaint at least 3 times a week for at least 3 months;
  • •be physically inactive (exercise less than 2 times a week).

排除标准

  • •evidence that insomnia is directly related to medical conditions or side effects os medications;
  • •obstructive sleep apnea syndrome;
  • •ECG abnormalities that prevent physical exercise or use of beta-blockers;
  • •uncontrolled clinical diseases (diabetes, hypertension, cardiovascular, neurological or renal diseases);
  • •use or history of abuse of alcohol or psychoactive substances;
  • •use of sleeping pills>2 times a week;
  • •shift workers.

研究组 & 干预措施

Exercise

Active Comparator

干预措施: Exercise (Behavioral)

Exercise + acupuncture

Experimental

干预措施: Acupuncture (Behavioral)

Exercise + acupuncture

Experimental

干预措施: Exercise (Behavioral)

结局指标

主要结局

Change from baseline anxiety to 12 weeks

时间窗: baseline, week 12

Prior sleep state anxiety will be assessed with the State-Trait Anxiety Inventory-STAI,25 the Portuguese version of which was validated by Gorenstein and Andrade.26 This scale encompasses 20 items and provides a one-dimensional measurement of anxiety. The volunteers were instructed to answer it 30 minutes before going to sleep at baseline and at the post-exercise evaluation.

Change from baseline quality of life to 12 weeks

时间窗: baseline, week 12

The SF-36 is a multidimensional questionnaire that covers eight components: physical functioning, role limitations due to physical health problems, role limitations due to emotional health problems, social functioning, vitality, general health perception, body pain, and mental health. All scores ranged from 0 to 100, with a higher score indicating better quality of life

Change from baseline mood to 12 weeks

时间窗: 12 weeks

The POMS questionnaire is an instrument to evaluate the acute profile of mood. It has 65 items and 6 domains: tension-anxiety, depression, anger-hostility, vigour-activity, fatigue, and confusion- bewilderment. The total mood disturbance score is derived by subtracting the vigour-activity score from the the sum of scores from the other subscales

Change from baseline insomnia to 12 weeks

时间窗: baseline, week 12

Insomnia Severity Index (ISI) was administrated at baseline and post treatment to assess insomnia-related complaints. It is a short and easy self-applied scale with 7 items scored from 0 to 4, with a total score varying from 0 to 28. The total score is interpreted as follows: absence of insomnia (0-7); sub-threshold insomnia (8-14); moderate insomnia (15-21); and severe insomnia

Change from baseline sleep diary to 12 weeks

时间窗: baseline, week 12

The sleep diary was used to evaluate the subjective perceptions of sleep. Participants were instructed to complete the diary every morning after waking for 1 week. The parameters evaluated were sleep onset latency, wake after sleep onset, total time in bed, number of arousals, sleep quality, feeling rested in the morning, and sleep efficiency (calculated retrospectively by the researchers as the ratio of reported total sleep time and reported total time in bed multiplied by 100 \[9\]). These data were averaged for each volunteer for pre- and post-treatment assessment weeks.

Change from baseline polysomnography to 12 weeks

时间窗: baseline, week 12

Polysomnographic recording included an electroencephalogram, an electrooculogram, an electromyogram, and an electrocardiogram. Measurements of air flow (oral and nasal), respiratory effort (thoracic and abdominal), body movement, and oxygen saturation were also taken. The measured variables included total sleep time, sleep efficiency (ratio between total sleep time and total recorded time multiplied by 100), sleep onset latency, wake after sleep onset, arousals, sleep stages (N1, N2 and N3 non-rapid eye movement \[non-REM\] sleep and REM sleep), latencies for each sleep stage. Two researchers who were blinded to the study design performed the staging and analysed the polysomnographic events using international criteria

Change from baseline sleep quality to 12 weeks

时间窗: baseline, 12 weeks

The PSQI assesses sleep quality over a 1-month period. The questionnaire consists of 19 self-rated questions and 5 questions that should be answered by bedmates or roommates. The latter questions are used only for clinical information. The 19 questions are categorized into 7 components, graded on a score that ranges from 0 to 3. The PSQI components are as follows: subjective sleep quality (C1), sleep latency (C2), sleep duration (C3), habitual sleep efficiency (C4), sleep disturbances (C5), use of sleeping medication (C6) and daytime dysfunction (C7). The sum of scores for these 7 components yields one global score, which ranges from 0 to 21, where the highest score indicates worst sleep quality. A global PSQI score greater than 5 indicates major difficulties in at least 2 components or moderate difficulties in more than 3 components.

次要结局

  • Change from baseline serum serotonin to 12 weeks(baseline, 12 weeks)
  • Change from baseline cortisol to 12 weeks(baseline, 12 weeks)
  • Change from baseline Effort eletrocardiogram test to 12 weeks(baseline, 12 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Giselle Soares Passos

Professor

Universidade Federal de Goias

研究点 (1)

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