Skip to content

12 weeks of strength training and high protein consumption in perimenopausal females

The combined effect of yogurt consumption with resistance exercise on body composition and inflammation in perimenopausal females

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN20867728
Enrollment
40
Registered
2026-01-08
Start date
2026-01-06
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Perimenopausal females Other

Interventions

This study has two nutrition supplement groups, which are consumed twice daily for 12 weeks. They consist of: 1. Intervention: 350 g high protein 0% Greek Yogurt 2. Energy and protein matched control

Sponsors

Dairy Farmers Of Canada
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Be in the perimenopausal period (Stage -1 or -2 assessed using the STRAW+10 guidelines) . 2. Be untrained/sedentary (<2 structured exercise sessions per week). 3. Low habitual dairy consumption (=1 serving of milk, yogurt, cheese/day). 4. Be able to maintain a habitual diet and safe to perform RET three times per week throughout the trial (assessed by the “Get Active” Questionnaire). 5. Understand the study procedures and provide informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Regular use of tobacco- or cannabis-related products (smoking, chewing or vaping). 2. Have any electronic medical or metal implants. 3. Currently pregnant or planning to get pregnant. 4. Allergy to dairy foods or lactose intolerance. 5. Orthopaedic conditions (MSK injury, chronic back pain etc) that may worsen with exercise. 6. Any acute or chronic illness relating to the cardiac, pulmonary, skeletal or neuromuscular systems, Type 1 diabetes or unmanaged hypertension, lipidaemia or cardiovascular disease or any other medical concern that may interfere with their ability to safely complete the study. 7. Regular use of medications known to affect protein metabolism or inflammation (i.e. corticosteroids, non-steroidal anti-inflammatory drugs (prescription use or daily use of over-the-counter medication), or prescription strength acne medications). 8. Concurrent participation in a research study that may interfere with the results of the current study.

Design outcomes

Primary

MeasureTime frame
Body composition measured using dual x-ray absorptiometry (DXA) at baseline and after 12 weeks

Secondary

MeasureTime frame
1. Skeletal muscle mass measured using D3-creatine at baseline and after 12 weeks 2. Skeletal muscle characteristics measured using muscle biopsy at baseline and after 12 weeks 3. Gut microbiome diversity from fecal samples measured using 16S gene sequencing at baseline and after 12 weeks 4. Menopausal symptoms, sleep, mood and GI disturbances measured by questionnaires (Menopause Specific Quality of Life Questionnaire, Pittsburgh Sleep Quality Index, Profile of Mood State, PROMIS-GI) at baseline and after 12 weeks 5. Muscle strength assessments measured using 5-Repetition Maximum (5RM) at baseline and after 12 weeks

Countries

Canada

Contacts

Public ContactJoel Prowting
prowtinj@mcmaster.ca+1 (0)905 525 9140 Ext. 21918

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026