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Cognicise Training for Seniors for Healthy Aging

P

Poznan University of Physical Education

Status

Completed

Conditions

Cardiopulmonary
Physical Fitness
Postmenopausal Women
Postural Stability
Elderly (People Aged 65 or More)
Blood Biomarkers
Fall Risk
Quality of Life
Depressive Symptom
Cognitive Functions

Treatments

Behavioral: Yoga Training
Behavioral: Cognicise Training

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this clinical trial is to assess the impact of two 8-week motor-cognitive exercise programs - Cognicise and yoga - on psychological, respiratory, cardiovascular, postural, and biochemical health in elderly women.

The main objectives are to evaluate whether these programs:

Improve psychological parameters such as mood, quality of life, depressive symptoms, and cognitive abilities;

Enhance respiratory function, including lung volumes and ventilation;

Influence cardiovascular parameters such as blood pressure and heart rate;

Improve chest mobility, physical fitness, and cardiorespiratory capacity;

Induce favorable changes in selected blood biomarkers, including neurotrophic factors, hormones, glucose, lipids, and blood morphology;

Improve postural stability, as assessed through posturographic analysis.

The study compares the effects of yoga and Cognicise to a control group that does not receive any intervention.

Participants in the yoga and Cognicise groups will take part in supervised sessions twice a week for 8 weeks (each session lasting 45 minutes).

Participants from all three groups (yoga, Cognicise, and control) will undergo pre- and post-intervention assessments, including:

Psychological questionnaires;

Spirometry and cardiorespiratory tests;

Blood pressure and heart rate measurements;

Chest mobility and physical fitness tests;

Posturographic assessment of postural control during quiet standing with eyes open and closed;

Laboratory blood tests (including BDNF, GDNF, 25(OH)D, TSH, testosterone, cortisol, insulin, glucose, lipid profile, and complete blood count with differential).

The aim is to determine whether structured motor-cognitive training leads to measurable health benefits compared to no intervention.

Enrollment

70 patients

Sex

Female

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

Women aged over 65 years; Community-dwelling; Score of at least 7 points on the Abbreviated Mental Test Score (AMTS).

Exclusion Criteria (presence of at least one of the following):

Locomotor system disorders preventing independent movement; Morbid obesity; Active or stable cancer (ongoing radiation or chemotherapy); Liver disease with ALT > 3× upper limit of normal; Chronic kidney disease (eGFR < 30 mL/min/1.73 m²); Acute inflammation (CRP > 5 mg/dL); Unstable ischemic heart disease; History of ischemic or hemorrhagic stroke within the last 6 months; History of STEMI with drug-eluting stent implantation; NSTEMI within the past 12 months; Inherited metabolic disorders (e.g., phenylketonuria, galactosemia); Autoimmune diseases (e.g., acute thyroiditis, celiac disease, systemic connective tissue disease, hemolytic anemia, vitiligo, Addison's disease, hyperbilirubinemia); Non-specific enteritis (e.g., Crohn's disease, ulcerative colitis); Psychological disorders; Current antibiotic therapy; Current steroid therapy.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 3 patient groups

Yoga Group
Experimental group
Description:
Participants in this group completed 16 yoga sessions over 8 weeks. Sessions were conducted twice a week and lasted 60 minutes each. Each session included a warm-up (15 minutes), a main part (30 minutes), and relaxation exercises (15 minutes). The practice focused on movements for the upper and lower limbs and the torso, especially the lumbar spine, pelvis, and hips. The final 10 minutes of each session were dedicated to achieving a deep relaxation state.
Treatment:
Behavioral: Yoga Training
Cognicise Group
Experimental group
Description:
Participants in this group completed 16 Cognicise training sessions over 8 weeks. Sessions were held twice a week and lasted 60 minutes. Each session followed a dual-task format combining motor and cognitive elements. Participants performed basic physical exercises while responding to live piano music and visual color cues. They also completed simple language tasks (e.g., spelling words backwards, naming items in categories) and arithmetic tasks. The session structure included a 15-minute warm-up, 30 minutes of cognitive-motor training, and 15 minutes of relaxation and breathing exercises.
Treatment:
Behavioral: Cognicise Training
Control Group
No Intervention group
Description:
Participants in the control group did not participate in any structured physical or cognitive training during the 8-week intervention period. They were instructed to maintain their usual daily routines and not to begin any new exercise or therapy programs. Baseline and post-intervention assessments were conducted at the same time points as in the intervention groups.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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