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CompletedNCT07158931Updated Sep 8, 2025

'Nordic Walking' on Geriatric Individuals

An interventional study of nordic walking and General walking in Geriatrics and Geriatric Rehabilitation, sponsored by Istanbul Rumeli University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 65 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-09-08.

Sponsored by Istanbul Rumeli University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 10 months after the study started (first participant enrolled Oct 2022, registered Aug 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
28
Allocation
Randomized
Ages
65 Years to 80 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Geriatrics
  • Geriatric Rehabilitation
03

In context

Lead sponsor

Istanbul Rumeli University is the lead sponsor of 26 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 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.

Exclusion criteria

Exclusion Criteria:

  • 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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
28 participants (actual)

Study arms

  • Experimental
    Experimental

    Nordic Walking

    Other: nordic walking

  • Active comparator
    Control

    General walking

    Other: General walking

Interventions

  • Othernordic walking

    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.

  • OtherGeneral walking

    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.

06

What researchers measure

Primary outcomes

  1. 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

    Time frame: at the beginning and at the end of the 12th week

  2. 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.

    Time frame: at the beginning and at the end of the 12th week

  3. 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.

    Time frame: at the beginning and at the end of the 12th week

  4. 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.

    Time frame: at the beginning and at the end of the 12th week

Secondary outcomes

  1. Tinetti Falls Efficacy Scale (TFES):

    It is a validated tool used to assess an individual's confidence in performing daily activities without falling. Participants rated their perceived safety during various daily activities on a scale from 1 (very confident) to 10 (not confident at all). Scores were converted to a total between 0 (low fall-related self-efficacy) and 100 (high fall-related self-efficacy), with higher scores indicating greater fear of falling (10).

    Time frame: at the beginning and at the end of the 12th week

  2. Tampa Kinesiophobia Scale (TKS):

    It is a 17-item self-report questionnaire rated on a 4-point Likert scale, designed to assess fear of movement or re-injury. Higher scores indicate greater levels of kinesiophobia.

    Time frame: at the beginning and at the end of the 12th week

  3. World Health Organization Quality of Life Instrument-Older Adults Module (WHOQL- OLD):

    It is a 24-item questionnaire assessed on a five-point Likert scale, covering six domains: sensory abilities, autonomy, past-present-future activities, social participation, death and dying, and intimacy. Each domain is scored from 4 to 20, and higher total scores indicate better quality of life

    Time frame: at the beginning and at the end of the 12th week

07

Study locations

1 site
  • Öziri
    Ataşehir, Istanbul, Turkey (Türkiye)
08

References and documents

Publications

  • Oziri N, Baskan E, Balkisli BC. Investigation of the effectiveness Of 'Nordic Walking' training on geriatric individuals: a randomized comparative study. Eur Geriatr Med. 2026 May 19. doi: 10.1007/s41999-026-01507-w. Online ahead of print. PubMed 42154148 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 8, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07158931
Lead sponsor
Istanbul Rumeli University
Responsible party
Nursel Oziri (PhD, Istanbul Rumeli University) — Principal investigator
First posted
Sep 8, 2025
Start date
Oct 1, 2022
Primary completion
Mar 1, 2024
Completion
Mar 29, 2024
Last update
Sep 8, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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