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Strength Training in Nonagenarians

Health Enhancing Strength Training in Nonagenarians

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00848978
Acronym
STRONG
Enrollment
60
Registered
2009-02-23
Start date
2009-03-31
Completion date
2009-09-30
Last updated
2019-09-13

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

Conditions

Elderly

Keywords

Functional capacity, Quality of life, Depression, Falls, Body composition, Physical activity

Brief summary

The Health Enhancing Strength Training in Nonagenarians (STRONG) is a randomised control trial to assess the effectiveness of an aerobic and strength training program for improving functional capacity and quality of life in nonagenarians. Sixty (51 women) nonagenarians (age range: 90-102 years) who live in a geriatric nursing home will be randomly assigned to either a usual care (control) group (n=30) or an intervention (training) group (n=30). Participants allocated in the usual care group will receive general physical activity guidelines and participants allocated in the intervention group will also enroll in three weekly non-consecutive individualized training sessions (\ 45-50 min each) during 8 weeks. The exercise program will consist of muscular strength \[with a special focus on leg press at 30% (start of the program) to 70% 1 repetition maximum (end)\] and aerobic exercises (cycle-ergometry during 3-5 to 15 minutes at 12-14 points in the rate of perceived exertion scale). Results from STRONG will help to better understand the potential of regular physical activity for improving the well-being of the oldest population groups.

Interventions

BEHAVIORAL8-week aerobic and strength training program

Participants allocated in the intervention group will be enrolled in three weekly non-consecutive training sessions for 8 weeks. Each session will last for about 45-50 min. The exercise program will consist of muscular strength and aerobic exercises. Each session will start and end with a low intensity \ 5-7 min warm-up and cool-down period respectively, consisting mainly of stretching exercises involving all major muscle groups.

Sponsors

Universidad Europea de Madrid
CollaboratorOTHER
Karolinska Institutet
CollaboratorOTHER
Hospital General Universitario Gregorio Marañon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
90 Years to 110 Years
Healthy volunteers
Yes

Inclusion criteria

* Age: 90 years or over. * Planning to stay in the same nursing home during the study. * Able to ambulate, with or without assistance. * Able to communicate. * Informed consent: Must be capable and willing to provide consent.

Exclusion criteria

* Acute or terminal illness. * Myocardial infarction in the past 3 months. * Not capable to ambulate. * Unstable cardiovascular disease or other medical condition. * Upper or lower extremity fracture in the past 3 months. * Severe dementia. * Unwillingness to either complete the study requirements or to be randomised into control or training group. * Presence of neuromuscular disease or drugs affecting neuromuscular function.

Design outcomes

Primary

MeasureTime frame
Functional capacity and quality of lifeAugust 2009

Secondary

MeasureTime frame
Depressive symptoms, falls and body compositionAugust 2009

Countries

Spain

Outcome results

None listed

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