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Effects of Exercise Training in Patients With Atrial Fibrillation and Sleep Apnea: A Pilot Study

Effects of Exercise Training in Patients With Atrial Fibrillation and Sleep Apnea: A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04562857
Enrollment
19
Registered
2020-09-24
Start date
2019-01-01
Completion date
2019-12-10
Last updated
2021-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Deprivation

Brief summary

Background: There are still many gaps in research concerning the effect of different physical training modalities on sleep deprivation in the population with different types of sleep apnea. Aims: The purpose of this study was to examine the effect of moderate-intensity interval training (MITT) on patients with different types of sleep apnea.

Detailed description

Methods: 15 Participants aged 45-65 years were randomized into two groups: obstructive sleep apnea group (OSA), and central sleep apnea group (CSA). The training lasted ten consecutive weeks with 30 uninterrupted sessions. The actigraph together with the Pittsburg sleep quality index (PSQI) was used in sleep quality assessment. 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, filled PSQI, and did 6MWT before the first and last training sessions.

Interventions

BEHAVIORALModerate intensity interval training (MITT)

interval exercises (intervention) on bicycle for patients with AF and OSA or AF with CSA for 10 weeks, 3 times/week for duration of 30-45 min/ session.

Sponsors

Swinburne University of Technology
CollaboratorOTHER
National Heart Institute, Egypt
CollaboratorOTHER_GOV
Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
45 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Patients who have AF confirmed by ECG 2. Their ages range from 45 and 65 years of age 3. Medically stable patients. 4. Current complaint of poor Sleep quality (SQ) (score \> 5 of the SQ scale) 5. Patients who have OSA or CSA confirmed by polysomnography

Exclusion criteria

* Any patient was known to have any unstable medical condition;or with any known musculoskeletal or neurological conditions that might interfere with the execution or the assessment of the exercise, was excluded from the study.

Design outcomes

Primary

MeasureTime frameDescription
Sleep quality scores (0 is best, 3 is worst)10 weeksdata about sleep from Pittsburgh sleep quality index questionnaire
sleep latency (in min)10 weekstime spent in bed before falling asleep (from the actigraph)
Total sleep time (in hours)10 weeksTotal time actually slept (from the actigraph)
Sleep fragmentation index (in %) (the more means worse)10 weeksIndex of the level of the sleep continuity (from the actigraph)
cutpoints10 weeksnumbers displayed on the actigraph to give a picture about activity level

Secondary

MeasureTime frameDescription
six minute walking distance (in meters)10 weeksrepresent aerobic capacity (distance walked in 6 min)

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026