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Recruiting NCT07163676

Is There a Response of Glaucoma to Baduanjin Exercise in Elders?

No phase Interventional Glaucoma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Baduanjin exercise.
Who it may be relevant to
Registry conditions: Glaucoma. Basic parameters: 65 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

glaucoma is prevalent between elders. Baduanjin exercise is a suitable exercise for elders. elders with glaucoma will divided to group I or group II. each/every group will contain 30 elders. group I will receive baduanjin exercise for 60 minutes every day ((except fridays) for eight weeks. group II will act as waistlist.

Detailed description

Baduanjin exercise is a suitable exercise for elders. elders with glaucoma will divided to group I or group II. each/every group will contain 30 elders. group I will receive baduanjin exercise for 60 minutes every day ((except fridays) for eight weeks. group II will act as waistlist.

Interventions

  • Behavioral Baduanjin exercise
    group I will receive baduanjin exercise for 60 minutes every day ((except fridays) for eight weeks.

Primary outcome measures

  • intraocular pressure [Time frame: it will be measured after 8 weeks]
Secondary outcome measures (5)
  • patient health questionnaire [Time frame: it will be measured after 8 weeks]
  • National Eye Institute Visual Function Questionnaire [Time frame: it will be measured after 8 weeks]
  • Glaucoma-related quality of life questionnaire [Time frame: it will be measured after 8 weeks]
  • State trait anxiety inventory [Time frame: it will be measured after 8 weeks]
  • Stress vulnerability scale [Time frame: it will be measured after 8 weeks]

Eligibility criteria

Inclusion criteria

  • high-tension primary open angle glaucoma (bilateral)
  • ocular hypertension in both eyes

Exclusion criteria

  • cataract
  • diabetes
  • cardiac disorders
  • obesity

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Cairo University — Giza

Identifiers

NCT: NCT07163676 · IRB00014233-35

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗