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Sleep Quality Response to Resisted Training After Coronary Artery Bypass Grafting

Not Applicable
Completed
Conditions
Sleep Deprivation
Interventions
Behavioral: exercise
Registration Number
NCT03853668
Lead Sponsor
Cairo University
Brief Summary

Background:There are still many gaps in research concerning the effect of different physical training modalities on sleep quality in the population underwent coronary artery bypass graft surgeries(CABG).Purpose:The present study was conducted to compare the quality of sleep in subjects who underwent CABG, were submitted to two types of training (i.e, aerobic exercise alone or combined aerobic and resistance training

Detailed Description

OBJECTIVE/BACKGROUND:

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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
80
Inclusion Criteria
  1. Patients who have underwent CABG surgery since 6-8 weeks
  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
  1. Any patient is known to have any unstable medical condition
  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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
aerobic exercise groupexerciseaerobic 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)
aerobic and resisted exerciseexercisecombined 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.
Primary Outcome Measures
NameTimeMethod
sleep quality to be assessed by Pittsburgh Sleep Quality Index (PSQI)up to 12 months

1.The Pittsburgh Sleep Quality Index (PSQI) is a self-report questionnaire that assesses sleep quality over a 1-month time interval.

sleep fragmentation index to be assessed by actigraphyup to 12 months

2.Actigraphy is a valid tool to assist in determining sleep patterns in normal, healthy adult populations, normal infants and children, and patients suspected of certain sleep disorders.

Secondary Outcome Measures
NameTimeMethod
Functional aerobic capacity to be assessed by 6 minute walk test (6MWT)6 months

The 6 Minute Walk Test is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity.

Trial Locations

Locations (1)

National heart institute

🇪🇬

Giza, Cairo, Egypt

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