Clinical trials

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Condition / disease
Location
Status: Not yet recruiting

Effects of Resistance and Dual-Task Training on Physical, Oculomotor, and Executive Functions in Older Adults With MCI

The goal of this clinical trial is to determine the effect of a combined therapeutic intervention program with anaerobic exercises (resistance exercises) and dual tasks on the physical, oculomotor, and executive functions of older adults with mild cognitive impairment. The main questions it aims to answer are: • How effective will a therapeutic intervention program combining resistance exercises with dual tasks be in improving the physical, oculomotor, and executive functions of older adults with mild cognitive impairment living in the community? Researchers will compare the effectiveness of a resistance exercise training program combined with dual tasks versus a resistance-only exercise training program to see if it improves the physical, oculomotor, and executive functions of older adults with mild cognitive impairment Participants Will: * Receive resistance exercises, resistance exercises combined with dual tasks. or the standard health care. The intervention programs will consist of 3 weekly sessions over 8 weeks. * Before the start and after the completion of the programs, they will be evaluated using a battery of tests. This includes sociodemographic and general health background, physical fitness tests, as well as assessments of executive functions and oculomotor Saccadic movements and anti-saccadic error. * be required to sign a consent form.

Participants needed: 66
Trial details
Age: 60-90Biological sex: AllType: InterventionalSponsor: Universidad Santo Tomas, ChileUpdated: Dec 11, 2025Locations: 2
Eligibility criteria

Men and women aged 60 years or older [+2]

Visual or auditory disability that impedes communication [+10]

Status: Not yet recruiting

Effectiveness of Exercise Plus Pain Neuroscience Education on Brain Function in Knee Osteoarthritis

A three-arm randomized controlled trial will be conducted. Fifty-nine participants with KOA will be recruited in a 1:1:1 ratio. Assessor, and statistician will be blinded to group allocation. One experimental group (n=19) will receive NME plus PNE, the other experimental group (n=19) will receive isolated NME and the control group (n=19) will continue with usual care. The PNE will be adapted to the context of the participants. Outcome measures will be brain activity, pressure pain threshold, pain intensity, disability, fear-avoidance beliefs, self-efficacy, and pain catastrophizing. Outcome measures will be evaluated pre-intervention, immediately post-intervention, and four-month post-intervention. The investigators hypothesize that there will be significant differences in favor of the NME plus PNE intervention group.

Participants needed: 57
Trial details
Age: 45+Biological sex: AllType: InterventionalSponsor: Universidad Santo Tomas, ChileUpdated: Jul 1, 2024
Eligibility criteria

women and men at least 45 years old radiologically diagnosed with unilateral or... [+1]

Patients who have received physical therapy or other conservative therapy in the... [+4]