12 Weeks Orienteering Program Exercise on Older Adults

December 3, 2023 updated by: Franclim Martins, University of Évora

Effects of Orientation Exercise Program on Older Adults, Motor Skills, Cognitive and Emotional State: a Pilot Study

This study aims to determine the effects of an orientation exercise program addressed to old on physical-motor, cognitive, and affective competencies.

This quasi-experimental study is a controlled trial involving an orientation exercise program. The program will run for 12 weeks (3 sessions per week).

Participants will be clustered into two groups: the experimental group will perform the exercise orientation sessions, and the control group will maintain regular activities routines. Evaluations will be performed before and after the intervention.

After the study is finished, the control group will attend a similar exercise program.

Study Overview

Status

Enrolling by invitation

Detailed Description

The aging process is lived for all and is associated with uncountable limitations, such as physical, psychological, cognitive, or emotional, that daily translate into difficulty in accomplishing normal activities (2). Simple tasks such as getting up and sitting, carrying a shopping bag, or climbing some stairs, start being seen as an obstacle, much because of aging and the associated decline in physical and cognitive competencies such as balance, limb strength, aerobic capacity, motor coordination, processing speed, memory, executive functioning and, consequently, affective competences, such as emotional states and depression may also be compromised (1).

Despite the above, it is known that there are some ways and alternatives that, even not reversing the aging process, might delay it, promoting healthy aging (6). Scientific advances recommend regular physical exercise since exercise ensures a more active lifestyle and, therefore, a less dependent on others' life. There are many options that physical exercise professionals can choose for planning physical exercise programs for older people (3).

Nonetheless, instead of exercise planning training prescription, other options can be used to achieve healthy aging. In alternative to traditional exercise training, sporting modalities, such as orientation, may benefit this population.

According to a study, after applying a protocol that included changes to the terrain to improve older adults' balance, there were significant improvements in their stride time (4).

Other studies done within the same area, which applied one questionnaire on functional well-being, and four scales on depression, gastrointestinal system, physical activity, and healthy index to senior athletes between the ages of 67 and 71, found significant improvements in all the referred parameters except for the depression scale where the control group made up of older adults who do not practice the modality showed better results (5).

However, the literature is scarce concerning the participation in orientation programs by the elderly population, namely in terms of this program's effect on aerobic capacity, lower limb strength, motor coordination, processing speed, memory, and executive functioning.

Study Type

Interventional

Enrollment (Estimated)

54

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Évora, Portugal
        • Universidade de Évora

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Aged 65-75 years old;
  • Locomotor independent capacity;
  • Independent living in the community;
  • Historical of physical activity practice;
  • Attended, at least, the 3º school grade.

Exclusion Criteria:

  • Cognitive impairment such < 15 points in Mini-Mental State Examination (MMSE);
  • Evidence of neuromuscular disturb;
  • Use of medication that conditions the performance of the orientation exercise tasks.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Non-Randomized
  • Interventional Model: Factorial Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental: Experimental Orienteering group program
The experimental group intervention will attend the orienteering program. The program integrates 3 sessions / week during 12 consecutive weeks.
Orienteering exercise program running for 12 weeks (30-45 minutes, 3 sessions/week). Sessions will have 4 phases: 1) Signature of attendance sheet; 2) warm-up exercises for 5 minutes; 3) Start of orienteering proofs, where the departs will occur individually, with 3 interval minutes between participants; 4) stretches session, to return to a calm state.
No Intervention: The control group

The control group will maintain the usually daily activities, not attending any exercise program.

After study end, the control group will have the opportunity to participate on an exercise program.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from the beginning, between groups comparison, in physical competencies
Time Frame: 0, 12 weeks
Fullerton Advance Balance Scale to assess balance, ranging from 0 (worst) to 40 (best) points
0, 12 weeks
Change from the beginning, between groups comparison, in physical competencies
Time Frame: 0, 12 weeks
Senior Fitness Test, 6 minutes walking to assess aerobic capacity, measure in meters
0, 12 weeks
Change from the beginning, between groups comparison, in physical competencies
Time Frame: 0, 12 weeks
Senior Fitness Test, Sit and Stand to assess limb strength, measure by the number of repetitions
0, 12 weeks
Change from the beginning, between groups comparison, in physical competencies
Time Frame: 0, 12 weeks
Soda Pop Test to assess motor coordination.
0, 12 weeks
Change from the beginning, between groups comparison, in cognitive competencies
Time Frame: 0, 12 weeks
Trail Making Test (Part A and B) to assess processing speed and executive functioning, measure in seconds
0, 12 weeks
Change from the beginning, between groups comparison, in cognitive competencies
Time Frame: 0, 12 weeks
Rey Auditory Verbal Test to assess memory, measure in seconds
0, 12 weeks
Change from the beginning, between groups comparison, in affective competencies
Time Frame: 0, 12 weeks
Profile of Mood States to assess mood states, ranging from -32 (best) to 200 (worst) points
0, 12 weeks
Change from the beginning, between groups comparison, in affective competencies
Time Frame: 0, 12 weeks
Geriatric Depression Scale to assess depression state, ranging from 0 (best) to 30 (worst) points
0, 12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cognitive impairment
Time Frame: 0 weeks
Mini-Mental State Examination, ranging from 0 (worst) to 30 (best) points
0 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Catarina Pereira, Doctoral degree, University of Évora
  • Principal Investigator: José Marmeleira, Doctoral degree, University of Évora

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 1, 2023

Primary Completion (Actual)

July 1, 2023

Study Completion (Estimated)

January 1, 2024

Study Registration Dates

First Submitted

June 22, 2023

First Submitted That Met QC Criteria

June 29, 2023

First Posted (Actual)

July 10, 2023

Study Record Updates

Last Update Posted (Estimated)

December 5, 2023

Last Update Submitted That Met QC Criteria

December 3, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • Franclim Martins

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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