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Enhancement of Physical Fitness in Older Adults

The Effectiveness of a Trainings Program on ADL Performance, Physical Fitness, Wellbeing, and Nocturnal Cramp in Elderly People

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01421628
Acronym
NLC2010
Enrollment
180
Registered
2011-08-23
Start date
2010-09-30
Completion date
2010-11-30
Last updated
2011-08-23

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

Conditions

Pain, Physical Impairment

Keywords

older adults, exercise, stretching, mobility

Brief summary

Ageing is related to a decrease in physical fitness, disability and age related symptoms like nocturnal leg cramps (NLC). Our research is focused on the enhancement of physical activity and mobility to increase physical fitness and decrease disability and nocturnal cramp in older adults.

Detailed description

The ageing population leads to an increase of chronic disease and disability and to a decrease of physical activity and ADL performance. This circle can be reversed by physical exercise to increase physical fitness. The goal of this research is to establish the effects of a trainings program on ADL performance, physical fitness and nocturnal cramps. Furthermore the characteristics from participants who benefit from the program will be investigated by the research. The study design is a randomized intervention study. Participants are elderly people, age 65 years and older, without cognitive impairment. Intervention: The intervention is a physical trainings program. The intensity is moderate, the frequency is daily and the total duration is 6 weeks. The control group will be provided with an education program. Main parameters are: physical fitness, nocturnal cramp severity and frequency.

Interventions

OTHERFitness exercise program

Exercise program, daily frequency, duration of 6 weeks.

Sponsors

University Medical Center Groningen
CollaboratorOTHER
Hanze University of Applied Sciences Groningen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* For patients to be included in our study, they had to experience regular episodes of NLC and are in good mental health. * The participants had to agree to the study protocol and complete the program. * After eligibility was verified, written informed consent was obtained.

Exclusion criteria

* Older adults taking quinine or sleep medication and those with orthopedic problems or with severe medical problems and co morbidity, which can cause muscular spasms and/or cramps.

Design outcomes

Primary

MeasureTime frameDescription
Physical fitnesssix weeksStrength, balance
ADL performancesix weeksPerformance based ADL test
Well beingsix weeksQuestionnaires like SF-36
Nocturnal crampsSix weeksVisual analogue scale (VAS)

Secondary

MeasureTime frameDescription
Frequency nocturnal crampSix weeksNumber of cramp attacks per day.

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026