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A Decision Aid for Patients With Age-related Cataract

Patient-centered and Economic Effectiveness of a Decision Aid for Patients With Age-related Cataract: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03992807
Enrollment
773
Registered
2019-06-20
Start date
2019-07-01
Completion date
2020-11-12
Last updated
2020-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Age-related Cataract

Brief summary

To determine whether a decision aid increases informed decision about cataract surgery for patients with age-related cataract.

Detailed description

The need for cataract surgery is on the rise globally due to the aging population and high demands for greater visual functioning. Patients with age-related cataract face their initial decision about when to undergo cataract surgery. Although the majority of patients want to participate in a shared decision-making process, no decision aid has been available to improve the quality of decision. The purpose of this study is to determine whether a decision aid increases informed decision about cataract surgery for patients with age-related cataract.

Interventions

Potential participants receive a printed decision aid booklet with information about cataract surgery choice, and outcome data will be gathered using standardized questions in a structured interview after 2 weeks and 1 year.

OTHERA usual education booklet

Potential participants receive a usual booklet about cataract and cataract surgery, and outcome data will be gathered using standardized questions in a structured interview after 2 weeks and 1 year.

Sponsors

Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Individuals aged 50-80 years who have been resident in the selected study district for more than six months; 2. A definite diagnosis of age-related cataract; 3. Having not received cataract surgery; 4. Willing to participate in the study and provide informed content.

Exclusion criteria

1. Bilateral blindness (presenting distance visual acuity worse than 3/60); 2. Having ocular, hearing or mental disorder precluding reading or telephone interview; 3. Ocular disorders other than cataract leading to permanent vision loss that could not be corrected through cataract surgery; 4. Having cataract surgery contraindication.

Design outcomes

Primary

MeasureTime frameDescription
Informed choice about cataract surgery (the proportion of participants who make an informed choice,which is defined as a good knowledge score and an intention that is consistent with their attitude score)2 weeks post interventionInformed choice is an aggregated measure of multiple measurements, including knowledge (a 12-item questionnaire that assesses conceptual (items 1-10) and numerical (items 11-12) knowledge), attitudes (6 items, with 5 responses for each), and intentions (single item with 5 responses) Analysis: Informed Choice= Good Knowledge (score ≥50% in basic knowledge, ≥40% in knowledge associated with each treatment option, and at least 1 point in each numerical knowledge question) AND Positive Attitude (score ≥24) AND Positive Intention (definitely will or likely to), OR Good Knowledge AND Negative Attitude (score \<23) AND Negative Intention (unsure, not likely to, or definitely will not)

Secondary

MeasureTime frameDescription
Perceived personal chances of surgical benefit/harms2 weeks post interventionParticipants will be asked about their perceived personal likelihood of experiencing specific outcomes if they have cataract surgeries, compared with an average patient who had undergone cataract surgery.
Decisional conflict2 weeks post interventionDecisional conflict will be assessed using a 16-item Decisional Conflict Scale.
Decisional confidence2 weeks post interventionDecisional confidence will be assessed using a 11-item Decision Self Efficacy Scale.
Time perspective2 weeks post interventionThis will be assessed using a 4-item short form of the Consideration of Future Consequences Scale, with five response categories ranging from strongly agree to strongly disagree.
Anticipated regret2 weeks post interventionTwo items from a validated scale will measure anticipated regret about having cataract surgery (action regret) and about not having cataract (inaction regret).
Cataract worry and anxiety2 weeks post interventionA validated single item will measure participants' level of worry about progression of cataract, using four verbal response categories ranging from not worried at all to very worried. Anxiety will be measured with a six-item short form.
Perceived importance of surgical benefit/harms2 weeks post interventionPurpose-developed items will be used to ask participants about their personal perceptions of the importance of specific outcomes in their decision-making about cataract surgery.
Undergoing cataract surgery1 year post interventionSelf-reported undergoing cataract surgery will be assessed via telephone survey at 1 year.
Decision regret1 year post interventionThe Decision Regret Scale will measure participants' level of regret regarding their initial decision whether to have cataract surgery or not.
Visual functioningBaseline, 1 year post interventionThis will be assessed using the Catquest 9SF questionnaire.
Fall questionnaire1 year post interventionThis will be assessed using a single item question Did you have any fall in the past 12 months whereby you landed on the ground or floor?
Heath-related quality of life: Chinese version of the EQ-5D-5L telephone interview scriptBaseline, 1 year post interventionThis will be assessed using the simplified Chinese version of the EQ-5D-5L telephone interview script from the EuroQol research foundation.
CostsBaseline, 1 year post interventionThis will be assessed using the Treatment Inventory of Costs in Patients with psychiatric disorders (TIC-P) questionnaire.
Booklet utilization and acceptability2 weeks post interventionAcceptability and utilization of materials will be assessed based on the following items: 1. the proportion of participants who could read the booklet all the way through; 2. the proportion of participants who agree that the information is new; 3. the proportion of participants who agree that the length is just about right; 4. the proportion of participants who think the information is balanced; 5. the proportion of participants who agree that the booklet is clear and easy to understand; 6. the proportion of participants who find the materials helpful; 7. the proportion of participants who feel it worth recommending to others.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026