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Completed

NCT Number: NCT03304535

Social Worker in an Eye-Care Service

The purpose of this research study is to determine whether involvement with a social worker helps reduce distress, depression, and increase patient activation in participants over a 6 month intervention period. The study will also describe common barriers to care that participants face.

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Key information

Conditions

Glaucoma Eye Diseases Ocular Hypertension

Sex eligibility

All sexes

Study type

Observational

Primary location

Wills Eye Hospital

Philadelphia, Pennsylvania, 19107, United States

About this study

An appointment will be scheduled for participant to meet with a social worker. The appointment may happen on day of participant's scheduled clinic appointment or on another mutually decided upon date and time. Should participant choose to participate, this first visit will be Visit 1 for the study.

Visit 1: Baseline

Informed consent will be obtained demonstrating an interest in participating.

A visit with the social worker will take place during Visit 1. This session will be held in a private office and allows participant time for discussion regarding any challenges, struggles and/or barriers they may be experiencing.

The following baseline questionnaires/surveys will be administered:

Modified Patient Activation Measure - measures participant confidence in taking care of their own health.

Distress Thermometer - measures participant distress level during the past week.

Patient Health Questionnaire -measures depression symptoms and severity if any.

Clinical information will be taken from participant's medical record. There may be follow-up questions related to data if information is unclear or incomplete.

Upon completion of Visit 1, participant will receive a satisfaction survey to evaluate how participant satisfaction with social worker interaction.

Social Worker Interventions: After Visit 1 and before Visit 2

The social worker will develop an intervention for participant during Visit 1 appointment. As many calls or in person meetings participant requires will take place. There will be no limit and it will be determined by participant's needs.

Visit 2: Follow-up After 6 Months

Upon completion of participant's six month follow-up in the study, the following questionnaires/surveys will be administered:

Modified Patient Activation Measure - measures how confident participant is at taking care of their own health.

Distress Thermometer - measures how much distress participant has been experiencing in the past week.

Patient Health Questionnaire - measures if participant has symptoms of depression and the severity of those symptoms.

Satisfaction Survey - measures how satisfied participant is with the social worker interaction.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients seen at Wills Eye Hospital in the Glaucoma Service
  • Glaucoma of any type, characterized by glaucomatous optic neuropathy and corresponding visual field (VF) defect
  • Referred to staff social worker for intervention
  • Ability to read, write, speak and understand English

Exclusion criteria

  • None

Treatment and study plan

Primary outcomes

  1. Change in response to Patient Health Questionnaire 9

    Time frame: 6 months

    Measures participant levels of depression based on questions related to depressive symptoms. The investigator will assess change in the number of participants with major, moderate, and minimal depressive symptoms.

Secondary outcomes

  1. Change in response to Distress thermometer

    Time frame: 6 months

    Measures participant level of distress on a scale of 1 to 10 and asks additional questions regarding contributors to distress.

  2. Change in response to Modified Patient Activation Measure 13

    Time frame: 6 months

    Measures participant self-capacity for and confidence regarding glaucoma management.

  3. Descriptive results of the Social Worker Baseline Assessment

    Time frame: 6 months

    Social worker will assess each participant's internal and external barriers to care, limitations, and strengths that may help them to manage their glaucoma.

Sponsors and collaborators

Lead sponsor

Wills Eye

Other

Registry information

Official study title

The Impact of a Social Worker in a Glaucoma Eye-Care Service: A Prospective Study

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Oct 9, 2017
Registry last updated
Oct 9, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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