Sleep Quality Response to Resisted Training After Coronary Artery Bypass Grafting
NCT ID: NCT03853668
Last Updated: 2019-02-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
80 participants
INTERVENTIONAL
2018-01-01
2018-07-01
Brief Summary
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Detailed Description
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There are still many gaps in research concerning the effect of different physical training modalities on sleep quality in the cardiac population. Thus, the objective of the present study was to compare the quality of sleep in subjects who underwent coronary artery bypass surgery submitted to two types of training (ie, aerobic exercise alone or combined aerobic and resistance training).
PATIENTS/METHODS:
80 Participants aged 45-65 years were randomized to two groups: aerobic group (AG), combined aerobic and resistance group (ARG). Training lasted ten consecutive weeks with 30 uninterrupted sessions. The actigraph (Actiwatch Minimitter Company, Incorporated (INC) - Sunriver, OR, USA) was placed on the non-dominant wrist and activities were monitored continuously while being recorded at one minute intervals. The participants kept the device for a period of 96 hours before the first and last training sessions.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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aerobic exercise group
aerobic exercises (intervention) on treadmill for 10 weeks, 3 times/week for duration of 30-45 min/session.
Exercise intensity is 50-65%of maximal heart rate (MHR)
exercise
control group (n=40) did aerobic exercises on treadmill for 10 weeks experimental group (n=40) did combined aerobic and resisted exercises for 10 weeks
aerobic and resisted exercise
combined resisted and aerobic exercises (intervention) for 10 weeks (circuit weight training and treadmill training respectively) 2 times/week for a duration of 30-45 min/session Exercise intensity is 50-65%of maximal heart rate (MHR) for aerobic part and 50% of 1 repetition maximum (1RM) for resistance part.
exercise
control group (n=40) did aerobic exercises on treadmill for 10 weeks experimental group (n=40) did combined aerobic and resisted exercises for 10 weeks
Interventions
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exercise
control group (n=40) did aerobic exercises on treadmill for 10 weeks experimental group (n=40) did combined aerobic and resisted exercises for 10 weeks
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Their ages ranges from 40 and 80 years of age
3. Medically stable patients.
4. patients did CABG-only treatment (not combined with valve replacement surgery)
5. Current complaint of poor Sleep quality (SQ) (score \> 5 of the SQ scale)
6. Body mass index ≤ 35 kg/m2 (no obstructive sleep apnea)
Exclusion Criteria
2. History of chronic insomnia for at least one year before surgery
3. Indication of receiving treatments for depression and anxiety
4. Musculoskeletal or neurological conditions that might interfere with the execution or the assessment of the exercise.
45 Years
65 Years
ALL
No
Sponsors
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Cairo University
OTHER
Responsible Party
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Hady Atef Labib
Assistant lecturer of physical therapy
Principal Investigators
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Hady Atef, Master
Role: PRINCIPAL_INVESTIGATOR
Assistant lecturer of physical therapy,Cairo University
Locations
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National heart institute
Giza, Cairo Governorate, Egypt
Countries
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Other Identifiers
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Sleep and exercise
Identifier Type: -
Identifier Source: org_study_id
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