'Nordic Walking' on Geriatric Individuals
Investigation of Effectiveness of 'Nordic Walking' Training On Geriatric Individuals: a Randomized Comparative Study
1 other identifier
interventional
28
1 country
1
Brief Summary
This study aimed to investigate the effects of Nordic Walking training on muscle strength and endurance, balance, fear of falling, aerobic capacity, fatigue, quality of life and activity level in geriatric individuals. 32 sedentary individuals between the ages of 65-80 participated in the study. Nordic Walking (NW) and Traditional Walking (GY) groups were created by systematic randomization method. In line with the intended research parameters, participants were given 30 sec sit-to-stand (30secCST), 30 sec biceps curl (30 sec ACT), timed up and go (TUG) 6 min walk (6MWT), Tinetti Fall Effectiveness (Tinetti FES), Tampa Kinesiophobia Scale (TSK), World Health Organization Quality of Life Elderly Module (WHOQOL-Old) were administered. Evaluations were repeated before and after the study. The study was conducted under the supervision of a physiotherapist, 3 days a week for 12 weeks in both groups.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 29, 2024
CompletedFirst Submitted
Initial submission to the registry
August 20, 2025
CompletedFirst Posted
Study publicly available on registry
September 8, 2025
CompletedSeptember 8, 2025
August 1, 2025
1.4 years
August 20, 2025
August 28, 2025
Conditions
Outcome Measures
Primary Outcomes (4)
Sit-to-stand test (STS):
This is a widely used clinical assessment tool in geriatrics for evaluating lower limb function, muscle strength, balance, and overall physical performance in older adults. Participants were instructed to sit on a chair approximately 48 cm in height, keeping their back straight, feet flat on the floor, and arms crossed over the chest. They were then asked to stand up and sit down repeatedly for 30 seconds. The total number of complete stands performed within the 30-second period was recorded
at the beginning and at the end of the 12th week
Biceps curl test (BCT):
This is a widely used assessment in geriatrics to evaluate upper body strength and endurance, particularly of the arm muscles (7). The arm curl test was performed with participants seated on a chair without armrests. Holding a dumbbell in the hand with the palm facing the body, participants executed elbow flexion with supination through a full range of motion, ensuring the elbow was fully bent and then fully extended for each repetition. Women used 2 kg dumbbells and men used 3 kg dumbbells. The total number of controlled repetitions completed in 30 seconds was recorded.
at the beginning and at the end of the 12th week
6-Minute Walk Test (MWT):
It is a widely used, simple, and validated clinical assessment to measure aerobic capacity and functional exercise tolerance in older adults (8). The participant was instructed to walk along a 30-meter flat surface for six minutes. At the end of the six-minute period, the total distance walked was recorded in meters.
at the beginning and at the end of the 12th week
Timed Up and Go Test (TUG):
This is a clinical and research tool to assess mobility, balance, walking ability, and fall risk in older adults (9). While seated on a chair approximately 48 cm in height, the participant was instructed, upon hearing the "start" command, to stand up, walk 3 meters forward at a normal walking speed, return, and sit down again. The test was performed twice, and the average time was recorded.
at the beginning and at the end of the 12th week
Secondary Outcomes (3)
Tinetti Falls Efficacy Scale (TFES):
at the beginning and at the end of the 12th week
Tampa Kinesiophobia Scale (TKS):
at the beginning and at the end of the 12th week
World Health Organization Quality of Life Instrument-Older Adults Module (WHOQL- OLD):
at the beginning and at the end of the 12th week
Study Arms (2)
Experimental
EXPERIMENTALNordic Walking
Control
ACTIVE COMPARATORGeneral walking
Interventions
Before the NW program, participants completed a one-week familiarization phase to practice pole use. Training was held three times: 15 minutes on days 1 and 2, and 20 minutes on day 3, at 40-60% heart rate reserve (measured with a pulse oximeter). Warm-up included a 1-minute slow walk, toe raises, seated dorsiflexion, mini squats, scapular adduction, and shoulder/wrist stretches. Each session ended with a cool-down of a 2-minute slow walk and 20-second stretches for major muscle groups (quadriceps, hamstrings, lumbar extensors, gastrocnemius, shoulders, wrists).The walking poles used in this study were the Evolite Ultralite Titanium Antishock Trekking Pole, which has a titanium alloy body and a three-piece telescopic structure, adjustable to the desired length between 68 and 135 cm.
The program was performed on concrete or compacted soil surfaces, under the same physiotherapist's supervision. Walking speed was adjusted to remain below 60% of maximal heart rate and to allow participants to converse comfortably during exercise.
Eligibility Criteria
You may qualify if:
- being between 65 and 80 years of age,
- having a score of 24 or above on the Standardized Mini-Mental State Examination (SMMSE),
- and voluntarily agreeing to participate in the study.
You may not qualify if:
- a history of cerebrovascular accident,
- acute retinal hemorrhage or previous ophthalmic surgery,
- active infection, malignancy,
- multiple organ failure, terminal illness, or a history of lower or upper extremity fracture within the last three months.
- had any musculoskeletal condition that would prevent them from engaging in exercise,
- a diagnosis of Alzheimer's disease, Parkinson's disease, or dementia,
- a diagnosis of benign paroxysmal positional vertigo (BPPV),
- had engaged in regular exercise training (≥150 minutes per week) within the past six months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Öziri
Ataşehir, Istanbul, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD
Study Record Dates
First Submitted
August 20, 2025
First Posted
September 8, 2025
Study Start
October 1, 2022
Primary Completion
March 1, 2024
Study Completion
March 29, 2024
Last Updated
September 8, 2025
Record last verified: 2025-08