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Comparison of Plus Lens Addition Versus Vision Therapy for Management of Accommodative Infacility

S

Superior University

Status

Active, not recruiting

Conditions

Accommodative Insufficiency

Treatments

Combination Product: Vision Therapy Using HART Chart
Diagnostic Test: Plus Lens Addition (+0.75 D)

Study type

Interventional

Funder types

Other

Identifiers

NCT06748534
MSRSW/Batch-Fall22/763

Details and patient eligibility

About

This Randomized Control Trials Study , conducted in Lahore, Pakistan, investigates the comparative efficacy of two approaches-plus lens addition of +0.75 diopters (D) and vision therapy using the HART chart-for managing accommodative infacility. Accommodative infacility, a condition characterized by the eye's reduced ability to adjust focus between distant and near objects, impacts both visual comfort and performance, particularly during prolonged near work.

Full description

The study sample comprises 38 participants, aged 15 to 35 years, divided into two groups: one group receiving plus lens addition of +0.75 D and the other undergoing structured vision therapy with the HART chart. Findings revealed that vision therapy was significantly more effective than plus lens addition, with results showing statistical significance at P < 0.05.

Enrollment

38 patients

Sex

All

Ages

15 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Participants aged 15 to 35 years.
  • Diagnosed with accommodative infacility.
  • Capable of adhering to the full study duration of 6 weeks.
  • Measurable accommodative dysfunction confirmed through baseline eye examinations.
  • Written informed consent from participants or guardians.

Exclusion criteria

  • Presence of other significant ocular or neurological conditions.
  • Inability or unwillingness to adhere to the prescribed treatment.
  • Prior treatment for accommodative infacility within the past 6 months.
  • Significant uncorrected refractive errors.
  • Medical contraindications for using plus lenses or vision therapy.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

38 participants in 2 patient groups

Interventional group I
Experimental group
Treatment:
Diagnostic Test: Plus Lens Addition (+0.75 D)
Interventional group II
Active Comparator group
Treatment:
Combination Product: Vision Therapy Using HART Chart

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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