University of Jaén
Jaén, JAEN, 23009, Spain
NCT Number: NCT07199114
This randomized, parallel-group clinical trial evaluates a 12-week adapted CrossFit program versus usual activity in community-dwelling older adults. The primary endpoint is change in Timed Up and Go (TUG) from baseline to 12 weeks. Secondary outcomes include Functional Reach (FRT), Romberg (eyes closed), gait velocity, stride length, and lower-limb power tests (Chair-Stand, Stair Ascent, Stair Descent; time and W/kg). Sixty participants were randomized (1:1). Analyses used repeated-measures ANOVA with Bonferroni adjustments and Cohen's d effect sizes.
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Notify Me65 year–80 year
All sexes
Interventional
Not applicable
Jaén, JAEN, 23009, Spain
Participants were screened and randomized (1:1) to an adapted CrossFit program (12 weeks) or to maintain usual activities (no structured training). Baseline characterization included demographics, anthropometrics, Mini-Mental State Examination (MMSE ≥ 26), physical activity level, and handgrip strength. Balance outcomes: Romberg (s, eyes closed), gait velocity (m/s), stride length (cm), TUG (s), and FRT (cm). Lower-limb power: Chair-Stand (s; W/kg), Stair Ascent/Descent (s; W/kg). Statistical analysis: normality (Shapiro-Wilk), homogeneity (Levene), repeated-measures ANOVA with Bonferroni post-hoc, and Cohen's d effect sizes. A priori sample size (G*Power 3.1): effect size 0.25, α = 0.05, power 0.80 → target n = 60 to account for attrition.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Community-dwelling older adults able to walk independently without assistance.
Cognitive function preserved, defined as a score of 26 points or higher on the Mini-Mental State Examination.
Absence of severe health conditions that would interfere with participation in exercise training.
Exclusion criteria
Presence of active neuromuscular or musculoskeletal disorders that prevent safe exercise participation.
Severe cardiovascular, pulmonary, or metabolic disease that contraindicates moderate-intensity exercise.
Any other medical or psychological condition that, in the opinion of the investigators, would make participation unsafe or unreliable.
Supervised sessions focused on functional, multi-joint movements adapted for older adults; emphasis on safety and progressive overload.
Time frame: Baseline and Week 12
Change in functional mobility. Shorter time indicates better performance and reduced risk of falls.
Time frame: Baseline and 12 weeks
Change in dynamic balance assessed by the distance a participant can reach forward without losing stability. Greater distance indicates better balance.
Time frame: Baseline and 12 weeks
Sit-to-stand repetitions (5 times). Lower time and higher relative power indicate better lower-limb strength and functional capacity.
Time frame: Baseline and week 12
Self-reported concern about falling during daily activities. Higher scores indicate greater fear of falling.
Time frame: Baseline and week 12
Subjective sleep quality over the previous month. Higher scores indicate poorer sleep quality.
Time frame: Baseline and week 12
Symptoms of anxiety and depression measured with HADS. Higher subscale scores indicate greater severity.
Time frame: Baseline and week 12
Walking speed measured over a standardized distance. Higher speed indicates better mobility.
Time frame: Baseline and week 12
Average step length during gait assessment. Longer stride indicates better gait performance.
Time frame: Baseline and week 12
Fear of movement measured with the Tampa Scale. Higher scores indicate greater kinesiophobia.
University of Jaén
Other
Strength Training and Modified CrossFit in Older Adults: a Comparative Perspective
Acronym: CrossfitUJA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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