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Traditional Exercise RCT in Visually Impaired Adults

N

Northeast Normal University

Status

Invitation-only

Conditions

Visual Impairments

Treatments

Behavioral: Taichi
Behavioral: Baduanjin

Study type

Interventional

Funder types

Other

Identifiers

NCT07265024
CCEE2026

Details and patient eligibility

About

This study aims to investigate the benefits and underlying mechanisms of traditional exercise interventions on the physical and mental health of individuals with visual impairments. A randomized controlled trial design will be employed, enrolling 90 visually impaired participants who will be randomly assigned to one of three groups: a Tai Chi intervention group, a Baduanjin intervention group, or a control group. The Tai Chi group will undergo a 12-week simplified 21-form Tai Chi training program, while the Baduanjin group will receive standardized Baduanjin training. The control group will participate in regular school physical education classes. Eligible participants are university students with visual impairments, defined as having visual acuity ≤ 0.05 or a visual field radius ≤ 10 degrees.

Enrollment

90 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • University students with visual impairment, defined as visual acuity ≤ 0.05 or a visual field radius ≤ 10 degrees.
  • Able to ambulate independently without assistance.
  • No severe cardiovascular diseases.

Exclusion criteria

  • Presence of severe physical illnesses or comorbid conditions that may affect participation.
  • History of psychiatric disorders.
  • Participation in other structured exercise training programs within the past three months.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

90 participants in 3 patient groups

Taichi
Experimental group
Treatment:
Behavioral: Baduanjin
Baduanjin
Experimental group
Treatment:
Behavioral: Taichi
Control Group
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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