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Effects of COVID-19 Lockdown in Exercising Early Postmenopausal Women

Effects of Three Months of COVID-19 Lockdown Induced Deconditioning After 13 Months of High Intensity Exercise Training in Early Postmenopausal Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04420806
Enrollment
21
Registered
2020-06-09
Start date
2020-03-14
Completion date
2020-10-30
Last updated
2020-11-13

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

Conditions

Detraining, Exercise, Muscle Atrophy, Muscle Weakness

Brief summary

While conditioning by exercise training has been widely evaluated, the available literature on passive deconditioning (i.e. forced deconditioning) is predominately limited to studies with or with almost complete mechanical and/or metabolic immobilization/sedation of the respective functional system (e.g. paralysis, bedriddenness). Vice versa, the effects of moderately long interruptions of dedicated types of exercise while maintaining everyday activity are rarely addressed. However, this topic is of high relevance, e.g. considering that breaks of health-related exercise programs due to increased family/occupational stress, vacation or temporary orthopedic limitation are rather frequent in everyday life. In the present project we aimed to determine the effects of 3 months of physical deconditioning due to COVID-19 induced lockdown after 13 month of high intensity endurance and resistance exercise in early postmenopausal women on parameters related to health and physical fitness.

Interventions

OTHERHIT-exercise

13 months of high intensity endurance and resistance exercise, 3x 45 min/week - 3 months of COVID-19 induced exercise break

OTHERSham intervention

Types of exercise (flexibility, relaxation) that did not affect the present outcomes

Sponsors

University of Erlangen-Nürnberg Medical School
Lead SponsorOTHER

Study design

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

Masking description

Outcomes assessors are unaware of participants group status and were not allowed to ask correspondingly

Intervention model description

One exercise versus one control group

Eligibility

Sex/Gender
FEMALE
Age
48 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* (early)postmenopausal women, ( normal menopause, 1-5 years post) * Osteopenia and osteoporosis (Bone Mineral Density \<-1.0 SD T-Score)

Exclusion criteria

* BMD \<-4.0 SD T-Score * Prevalent clinical, low-trauma fractures * Diseases and drugs with relevant effects on bone and muscle metabolism (e.g. glucocorticoids \>7.5 mg/d or bisphosphonate therapy); individual case assessment * Diseases and drugs with relevant effects on cardiometabolic risk factors (e.g. severe hypertension with corresponding medical therapy); individual case assessment * Severe cardiovascular events (e.g. stroke, coronary infarction) in the past. * Other conditions, diseases that exclude exercise training or testing

Design outcomes

Primary

MeasureTime frameDescription
Body compositionFrom intervention end to 3 months FUBody composition as determined by Dual-Energy x-Ray Absorptiometry

Secondary

MeasureTime frameDescription
Hip-/Leg extension strengthFrom intervention end to 3 months FUHip-/Leg extension strength as determined by an isokinetic leg press
Metabolic SyndromeFrom intervention end to 3 months FUcardio-metabolic risk factors summarized in the Metabolic Syndrome Z-Score according to the definition of the International Diabetes Federation
Bone Mineral Density (BMD)From intervention end to 3 months FUBMD at the lumbar spine and total hip as determined by Dual Energy x-Ray Absorptiometry
Menopausal symptomsFrom intervention end to 3 months FUMenopausal symptoms as determined by the Menopausal Rating Scale (MRS) with a scale from 0 (no complaints) to 4 (very serious complaints).
Back and joint painFrom intervention end to 3 months FUBack and joint pain as determined by a standardized pain questionnaire with a scale from 0 (never) to 7 (permanent) for pain frequency or 0 (no pain) to 7 (extremely) for pain severity.

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026