Crossfit in Special Population

NCT ID: NCT07199114

Last Updated: 2025-09-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-02-01

Study Completion Date

2025-07-01

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Postural Balance Strength Training Adaptations Aging

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Adapted CrossFit Program

Supervised, scaled functional multi-joint training tailored to older adults, combining strength and metabolic conditioning with progressive overload over 12 weeks.

Group Type EXPERIMENTAL

Adapted CrossFit Program (12 weeks)

Intervention Type BEHAVIORAL

Supervised sessions focused on functional, multi-joint movements adapted for older adults; emphasis on safety and progressive overload.

Usual Activity (Control)

Participants maintain habitual daily activities with no structured training.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Adapted CrossFit Program (12 weeks)

Supervised sessions focused on functional, multi-joint movements adapted for older adults; emphasis on safety and progressive overload.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.
Minimum Eligible Age

65 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Jaén

OTHER

Sponsor Role lead

Responsible Party

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DAVID CRUZ DÍAZ

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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University of Jaén

Jaén, JAEN, Spain

Site Status

Countries

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Spain

Other Identifiers

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CrossfitUJA

Identifier Type: -

Identifier Source: org_study_id

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