Audio-guided Home Physical Activity to Support People With Low Vision: Physical Performance and Quality of Life

Sponsor
Istituti Clinici Scientifici Maugeri SpA (Other)
Overall Status
Recruiting
CT.gov ID
NCT05956730
Collaborator
(none)
15
1
2
37.8
0.4

Study Details

Study Description

Brief Summary

The aim of the project is to investigate the effectiveness of a home training managed through audio-guides in comparison to a classic supervised training on the physical and psychological parameters of patients with severe low vision.

In this study the feasibility and effectiveness of a self-managed physical activity protocol with audio guides on physical performance (strength, mobility and aerobic capacity) will be assessed and compared to the same protocol supervised in a fitness environment.

Secondary aims are the effects of the two types of administration of the protocol on quality of life, autonomy and psychological impact on the caregiver.

Condition or Disease Intervention/Treatment Phase
  • Other: Physical Activity (AUD)
  • Other: Physical Activity (SUP)
N/A

Detailed Description

According to the World Health Organization, low vision is that condition of permanent reduction of the visual function which does not allow an individual to fully develop his relationship activity, conduct a normal work activity, pursue his needs and aspirations of life. The increase in life expectancy on the one hand and the increasingly better ability to prevent and treat serious eye diseases, has led in industrialized countries to extraordinarily high numbers of patients who develop serious hypovision in adulthood or advanced age.

Since regular physical activity is essential for maintaining good health in older adults, even those with limited mobility, to maintain muscle mass and good balance (thus preventing falls) the use of audio devices or workouts carried out through audio guides for management of exercises in autonomy and at home will be tested. The aim of the project is to investigate the effectiveness of a home training protocol managed through audio-guides, in comparison to a classic supervised training, on the physical and psychological parameters of patients with severe low vision.

Participants (people with severe low vision) will be randomized into two groups: "audio" group (AUD), trained through exercises explained through audio files and "supervised" group (SUP), trained in a gym supervised by a personal trainer.

The training protocol will have a total duration of 3 months, with 2 weekly sessions and a monthly re-planning of loads and intensities.

The participants of the SUP group will be trained at the Adapted Motor Activity Laboratory (LAMA) of the University of Pavia.

To evaluate the changes induced by exercise, subjects will undergo physical tests and questionnaires, at the beginning and monthly until the end of the study.

It is expected that combined training should increase aerobic capacity and general strength of the individual, as well as have a positive effect on quality of life and psychosocial life, both using audio-guided and supervised training.

Obtaining these benefits with a self-managed training strategy would lead to greater independence of the subject and would expand the possibility of intervention in the population with low vision. Ultimately, these benefits could also be reflected in the management of the person with low vision by the caregiver and close family members.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
15 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Audio-guided Home Physical Activity to Support People With Low Vision: Physical Performance and Quality of Life
Actual Study Start Date :
Nov 4, 2020
Anticipated Primary Completion Date :
Oct 30, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group 1

The proposed protocol includes a part of aerobic training and a subsequent part of strengthening exercises for large muscle groups. The total duration of each session will be approximately 30 minutes. There are 2 weekly training sessions for 3 months.

Other: Physical Activity (AUD)
Home training of patients with severe low vision managed through audio-guides (AUD).

Active Comparator: Group 2

The proposed protocol includes a part of aerobic training and a subsequent part of strengthening exercises for large muscle groups. The total duration of each session will be approximately 30 minutes. There are 2 weekly training sessions for 3 months.

Other: Physical Activity (SUP)
Training of patients with severe low vision in a gym supervised by a personal trainer (SUP).

Outcome Measures

Primary Outcome Measures

  1. Timed up and go - version for the visually impaired (TUG-LV) [3 months]

    Assessment of functional walking ability. In this version for patients with visual impairments, the subject must get up from the chair and walk 6 meters to a luminous point (light point) and go back to sit down as quickly as possible.

Secondary Outcome Measures

  1. Sit to stand test (1-MSTS) [3 months]

    Functional evaluation of muscle power. Sitting on a chair without armrests (about 50cm high) and with his hands on his chest, the patient must get up and sit down as quickly as possible, as many times as possible within 1 minute.

  2. Sit and reach test (SR) [3 months]

    Flexibility of the subject's posterior muscle kinetic chain. The subject seated with legs extended on the floor, with bare feet resting on a specific graduated cube, exhales and slowly bends the torso forward (without bending the knees) and tries to reach the farthest point of the cube with his own fingers.

  3. 3 minutes step test (3MST) [3 months]

    Assessment of aerobic capacity. Using a 15 cm high step (step), the subject is asked to go up and down the step as many times as possible in 3 minutes. The correct repetitions are recorded, i.e. when in the transition from the ground to the step and vice versa, both feet are on the ground and the knees are extended.

  4. hand-grip test [3 months]

    assessment of generic strength (isometric specification of the hand flexors). The subject seated with his elbow resting on the table (respecting the angles between the bust and forearm according to the guidelines) squeezes a dynamometer with as much force as possible.

  5. Berg Balance Scale [3 months]

    assessment of proprioceptive and balance skills through the execution of dynamic movements and the maintenance of static postures, in order to obtain information on the subject's motor skills, on the possible need for walking aids and on the risk of fall it presents

  6. Satisfaction Profile (SAT-P) questionnaire [3 months]

    level of personal satisfaction and quality of life.

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Residual visus up to 1/10 or residual binocular perimeter less than 30% (Severely visually impaired);

  • age greater than or equal to 50 years;

  • sedentary lifestyle, PASIPD questionnaire value less than 13.2 Mets hours/day;

  • sedentary lifestyle, IPAQ-SF questionnaire value less than 700 Mets/week;

  • absence of autonomous mobility with white cane.

  • proprioceptive and balance skills such as to allow the protocol to be managed independently and safely, value of the Berg Balance Scale test greater than 35.

Exclusion Criteria:

Subjects who report habitual physical activity or sports;

  • PASIPD questionnaire value greater than 13.2 Mets hours/day.

  • Subjects at high risk of falling, with a Berg Balance Scale test value of less than

  • Subjects with pathologies that are not compatible with carrying out the physical activity protocol in safety and autonomy.-

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istituti Clinici Scientifici Maugeri Pavia Italy 27100

Sponsors and Collaborators

  • Istituti Clinici Scientifici Maugeri SpA

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Istituti Clinici Scientifici Maugeri SpA
ClinicalTrials.gov Identifier:
NCT05956730
Other Study ID Numbers:
  • 2422
First Posted:
Jul 21, 2023
Last Update Posted:
Jul 21, 2023
Last Verified:
Jul 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Istituti Clinici Scientifici Maugeri SpA
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 21, 2023