Evaluating The Effectiveness Of Structured Psychosocial Counseling On Mental Health And FI Individuals With Low Vision

N/AActive Not RecruitingNCT06914076

Superior University28 enrolled

Overview

Vision impairments affect 2.2 billion people worldwide, including 36 million who are blind and 217 million with moderate-to-severe visual impairment. In the US, age-related vision loss is a leading cause of disability among older adults.

With increasing longevity, global blindness rates are expected to triple, and moderate-to-severe vision impairment rates to double in 30 years. The study aims to assess the effects of structured psychosocial counseling on mental health (depression, anxiety) and functional independence in individuals with low vision. Additionally, it seeks to evaluate the overall impact on quality of life (QoL) following the counseling intervention. A randomized controlled trial will be conducted at Superior University Lahore.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

HEALTH_SERVICES_RESEARCH

Masking

NONE

Enrollment

Conditions

Low Vision

Interventions

Structured Psychosocial CounselingCOMBINATION_PRODUCT

"Group A (Experimental Group): Participants in the Experimental group will be divided into groups with the persons having visual acuity 6/60, counting fingers and light perception will receive low vision aids etc and structured psychosocial counseling tailored for individuals with low vision. Counseling will be delivered over a 12-week period, consisting of weekly 60-minute sessions conducted by trained counselors. The program will focus on the following: Coping mechanisms for depression and anxiety. Strategies to improve functional independence and daily living skills. Social integration techniques to enhance participation in community activities. Low visions aids under supervision of low vision specialist."

Standard CareDIAGNOSTIC_TEST

Group B (Control Group): The control group will continue receiving standard care, including referrals and informational support.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 80 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Individuals aged 18 to 80 years. * Both male and female * Individuals diagnosed with low vision, defined as a visual acuity of less than 6/18 but equal to or better than 3/60 in the better eye with best correction. * Individuals having visual acuity 6/60, Counting fingers or light perception. * Individuals experiencing symptoms of depression or anxiety as assessed through a validated screening tool. * Individuals reporting reduced functional independence in daily activities due to low vision. Exclusion Criteria: * Unable to provide informed consent. * Diagnosed with severe psychiatric disorders such as schizophrenia, bipolar disorder, or severe post-traumatic stress disorder. * Existing involvement in similar counseling programs. * Presence of medical conditions or disabilities. * Pregnant individuals if pregnancy-related complications or responsibilities could interfere with participation in the intervention.

Locations (1)

Dial hospital, Qadirabad road Ali pur chattah

Guiranwala, Punjab Province, Pakistan

Outcomes

Primary Outcomes

DASS 21

The DASS-21 uses the following categories to interpret scores: Normal: 0-9 (Depression), 0-7 (Anxiety), 0-14 (Stress) Mild: 10-13 (Depression), 8-9 (Anxiety), 15-18 (Stress) Moderate: 14-20 (Depression), 10-14 (Anxiety), 19-25 (Stress) Severe: 21-27 (Depression), 15-19 (Anxiety), 26-33 (Stress) Extremely Severe: 28+ (Depression), 20+ (Anxiety), 34+ (Stress)

Time frame: 12 Months

LVQoL Questionare

Total Score Interpretation: * 25-50: Good quality of life * 51-75: Moderate quality of life * 76-100: Poor quality of life * 101-125: Very poor quality of life

Time frame: 12 Months

Data from ClinicalTrials.gov

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