Short-term Circuit Training on Muscle Mass and Quality of Life in Sedentary Postmenopausal Women

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-75
SponsorLoma Linda University

About this trial

The purpose of this graduate student research study is to provide healthcare professionals with evidence of the potential of circuit strength training in improving the physical and psychosocial well-being of postmenopausal women.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Females aged between 50 and 75 years.

Self-reported postmenopausal status (i.e., cessation of menstruation for a minimum of 12 months).

Physically capable of participating in an exercise intervention.

No engagement in structured resistance or aerobic training programs in the six months preceding the study.

Disqualifiers

Classification as moderate and highly active on the International Physical Activity Questionnaire (IPAQ) (600-3000 MET-minutes/week for "moderate" and higher than 3000 MET-minutes/week for "high" score)

Diagnosis of any health condition that constitutes a contraindication to physical exercise (e.g., significant cardiovascular disease, orthopedic or neuromuscular restrictions impacting exercise performance or safety).

Regular use of medication with the potential to affect study outcomes (e.g., corticosteroids, immunosuppressants).

Trial design

Design model

Parallel

Treatments tested in this trial

  • Exercise

    Other intervention

    The protocol involves a 10-minute warm-up and cool-down session, followed by two sets of high-intensity circuit training exercises (bench press, squats, overhead press, calf raising, barbell row, deadlifts) that last 12 minutes each (6 stations×2sets). There will be a 3-minute break between the exercise sets. The heart rate required during the exercise will be between 70-90% of their maximum capacity and a pre-scale rate of 7.5. The intensity of the exercise will be progressive each two weeks, commencing at 50% of their one rep max and increasing to 80% in their last week. During the initial phase, participants will be required to complete eight reps for each exercise. We will encourage them to increase their intensity level every two weeks.

  • No exercise

    Other intervention

    This group will need to maintain their sedentary lifestyle without changing their activity levels or diet

Treatment groups

46 Participants
are divided into 2 treatment groups
Group A: Exercise GroupExperimental treatment 1 intervention
Group B: Non-Exercise GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

sleep quality

The Pittsburgh Sleep Quality Index will be used to measure any trouble sleeping.

Time frame
change between baseline and eight weeks
2

IL-6 Biomarker

Inflammatory biomarker IL-6 will be tested using a blood draw.

Time frame
change between baseline and eight weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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