Effects of Zero-Time Exercise (ZTEx) on Inactive Adults With Insomnia

Insomnia, Primary Clinical Trial

Official title:

Effects of Zero-Time Exercise (ZTEx) on Inactive Adults With Insomnia: A Pilot Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03155750
• Other study ID #: ZTEInsomnia
• Status: Completed
• Phase: N/A
• First received: May 14, 2017
• Last updated: October 18, 2017
• Start date: June 5, 2017
• Est. completion date: September 7, 2017

Study information

• Verified date: October 2017
• Source: The Hong Kong Polytechnic University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Objectives: To evaluate the clinical effects of Zero-Time Exercise (ZTEx) for treating insomnia disorder delivered by a training course.

Hypothesis: Subjects in the ZTEx training group will have greater improvement in insomnia symptoms and daytime impairment than those in the sleep hygiene education (SHE) group at week 8.

Design and subjects: A randomized controlled trial. 32 inactive subjects with insomnia disorder recruited from the community will be randomized to ZTEx training or SHE groups in a 1: 1 ratio.

Study instrument: Insomnia Severity Index (ISI) will be used to assess insomnia symptoms and daytime impairment.

Interventions: Subjects in the ZTEx training group will attend two training lessons (2-hour each) to learn ZTEx and practice it every night for 8 weeks; subjects in the SHE group will receive sleep hygiene education with the schedule and duration that are same to the ZTEx training group.

Main outcome measures: The primary outcome measure is the ISI score. Other measures include sleep parameters by subjective sleep diary and objective actigraphy, Hospital Anxiety and Depression Scale, Multidimensional Fatigue Inventory-20 and Short Form-6 Dimension. Acceptability and compliance of ZTEx will be evaluated.

Data Analysis: Differences in the questionnaire scores, subjective and objective sleep parameters will be examined using a mixed-effects model.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 37
• Est. completion date: September 7, 2017
• Est. primary completion date: September 7, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Adults age 18-65 years old;

• Chinese Hong Kong residents who are able to communicate in Cantonese or Mandarin;

• A current clinical Diagnostic and Statistical Manual of Mental Disorders-fifth edition (DSM-5) diagnosis of insomnia disorder (Primary in nature) according to the Brief Insomnia Questionnaire (BIQ), a validated diagnostic tool. The criteria include having difficulties in falling asleep, difficulties in staying asleep, or early morning awakening with clinically significant consequences for daily life for at least 3 months;

• Insomnia Severity Index total score of at least 10 indicating insomnia at the clinical level;

• Willing to give informed consent and comply with the trial protocol;

• Ambulant and independent in activities of daily living;

• Physically inactive which refers to less than 150 minutes moderate-intensity activity per week or less than 75 minutes vigorous-intensity activity per week, or an equivalent combination of moderate- and vigorous- intensity activity.

Exclusion Criteria:

• Evidence of association of insomnia with medical conditions, other sleep disorders, or side-effects of medications;

• Use of medication or psychotherapeutic components for insomnia or other psychiatric disorders;

• Other possible psychiatric disorders including generalized anxiety disorder (GAD), major depressive disorder (MDD), posttraumatic stress disorder (PTSD), psychosis as screened by structural clinical interview of DSM-IV;

• cognitive impairment preventing informed consent or understanding of instructions (score < 22 in Montreal Cognitive Assessment Hong Kong version);

• Shift work;

• body mass index equal to or over 27.5, the obese criteria for Asians;

• Unsafe conditions or incapable to exercise as recommended by their physician.

Related Conditions & MeSH terms

• Insomnia, Primary
• Sleep Initiation and Maintenance Disorders

Intervention

Other:
• Zero Time Exercise
Zero Time Exercise encourage people to increase physical exercise by simple movements that can be done any time at any places. We offer a 2-session training course to train the subjects to do zero-time exercise.
• Sleep hygiene education
We offer a 2-session education course to teach the subjects about sleep hygiene practice.

Locations

Country	Name	City	State
Hong Kong	School of Nursing, the Hong Kong Polytechnic University	Hong Kong

Sponsors (1)

Lead Sponsor	Collaborator
The Hong Kong Polytechnic University

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Insomnia Severity Index	The subjects rate the severity of insomnia, the distress, and the functional impairment associated with insomnia on a 5-point	week 8
Secondary	Sleep diary (7-day)	The standardized sleep diary records the daily bedtime and rising time, from which the total time in bed (TIB) can be calculated.	Baseline, week 4, week 8
Secondary	Multidimensional fatigue inventory-20	Multidimensional fatigue inventory-20 is a 20-items self-report instrument designed to measure severity of fatigue.	Baseline, week 4, week 8
Secondary	Hospital Anxiety and Depression Scale	The Hospital Anxiety and Depression Scale is a 14-items self-administered questionnaire, which assesses the severity of depressive and anxiety symptoms	Baseline, week 4, week 8
Secondary	Actigraphy (7-day)	Actigraphy measures wrist movements to assess sleep or waking state, is accomplished through an accelerometer in a wrist worn device	Baseline, week 8
Secondary	Short Form-6 Dimension	The Short Form-6 Dimension is composed of six multi-level dimensions to assess the quality of life which can be used in cost-utility analysis.	Baseline, week 4, week 8
Secondary	Hand grip strength	Objective hand grip strength	Baseline, week 8
Secondary	Level of activity	Self-report level of activity in moderate and vigorous intensity	Baseline, week4, week 8
Secondary	Weight	Weight in kilograms; (Weight and Height will be combined to report as BMI in kg/m^2)	Baseline, week 8
Secondary	Height	Height in meters; (Weight and Height will be combined to report as BMI in kg/m^2)	Baseline, week 8