Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00013416 · ClinicalTrials.gov registry record · Phase 2

Measurement and Prediction of Outcomes of Amplification

A Phase 2 study, sponsored by US Department of Veterans Affairs.

Completed
Registry status
Phase 2
Development phase
120
Enrollment target

NCT00013416: Completed Phase 2 study, sponsored by US Department of Veterans Affairs.

NCT00013416 is a Phase 2 study that has completed, run by US Department of Veterans Affairs. The registered enrollment target is 120 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (10% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00013416, a Phase 2 study, has completed, sponsored by US Department of Veterans Affairs.

COMPLETED
Registry status
Phase 2
Development phase
120 participants
Enrollment target

Study Summary

The long-term goal of this research program is to develop methods to predict both the benefit and the satisfaction that hearing-impaired patients will derive from auditory amplification in daily life. This proposal has three primary objectives: (1) To determine the influence of extra-audiological variables, such as personality attributes and expectations, on the subjective outcomes of hearing aid fittings, (2) To establish a scientific basis for selection, administration, and interpretation of self-report measures of hearing aid fitting outcome, (3) To resolve the long-standing debate about the efficacy of using clinically measured loudness perception data in hearing aid prescriptions.

Interventions

  • PROCEDURE Hearing

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 1999-10
Est. Completion 2002-09
Phase Phase 2
US Department of Veterans Affairs

632 total trials

What the finished NCT00013416 record still lists

NCT00013416 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (10% lower).

The record links to 0 conditions, and to 1 intervention - of which Hearing is the first listed.

NCT00013416 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00013416 about?

NCT00013416 is a clinical study titled "Measurement and Prediction of Outcomes of Amplification". The long-term goal of this research program is to develop methods to predict both the benefit and the satisfaction that hearing-impaired patients will derive from auditory amplification in daily life. This proposal has three primary objectives: (1) To determine the influence of extra-audiological va...

What is the current status of trial NCT00013416?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 120 participants. The study started on 1999-10. Estimated completion is 2002-09.

What interventions are being tested in trial NCT00013416?

The interventions under investigation include: Hearing (PROCEDURE).

Who is sponsoring clinical trial NCT00013416?

This trial is sponsored by US Department of Veterans Affairs, which has 632 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00013416's enrollment target sits among peer trials

120 569th of 2000 higher than 1,383 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01174108 · 120 participants · Phase 2

    Allogeneic Hematopoietic Stem Cell Transplantation for Severe Aplastic Anemia and Other Bone Marrow Failure Syndromes Using G-CSF Mobilized CD34+ Selected Hematopoietic Precursor Cells Co-Infused With a Reduced Dose of Non-Mobilized Donor T-cells

  • NCT01627301 · 120 participants · NA

    Sympathetic Overactivity in Post-traumatic Stress Disorder

  • NCT02025023 · 120 participants · Phase 3

    Local 5-Fluorouracil Injection for the Treatment of Chalazia: A Prospective, Comparative Study

  • NCT02128906 · 120 participants · Phase 2

    Radiotherapy With Cisplatin vs. Docetaxel-cetuximab in HNSCC: ERCC1 Biomarker Enrichment and Interaction Design

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00013416, the US trial registry maintained by the National Library of Medicine. NCT00013416 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.