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

NCT01934621 · ClinicalTrials.gov registry record · NA

Adapting Daily Activity Performance Through Strategy Training

A NA study, sponsored by University of Pittsburgh.

Completed
Registry status
NA
Development phase
128
Enrollment target

NCT01934621: Completed NA study, sponsored by University of Pittsburgh.

NCT01934621 is a NA study that has completed, run by University of Pittsburgh. The registered enrollment target is 128 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01934621, a NA study, has completed, sponsored by University of Pittsburgh.

COMPLETED
Registry status
NA
Development phase
128 participants
Enrollment target

Study Summary

Individuals with cognitive impairments after stroke sustain significant disability in their daily tasks, and account for a significant proportion of stroke-related healthcare costs. The proposed study examines a novel intervention, strategy training, that shows promise for helping individuals with stroke-related cognitive impairments reduce disability in daily tasks, which may lead to reductions in healthcare costs. We predict that strategy training will result in significantly greater independence 6 months after stroke compared to an attention control intervention, and that strategy training may reduce cognitive impairments.

Primary Outcome

Moderate effect size of difference between groups in independence (measured with the Functional Independence Measure)

Interventions

  • BEHAVIORAL Strategy Training
  • BEHAVIORAL Attention Control

Trial Details

FieldValue
Enrollment Target 128 participants
Start Date 2013-11
Est. Completion 2020-09
Phase NA
University of Pittsburgh

1,238 total trials

What the finished NCT01934621 record still lists

NCT01934621 is an interventional study that assigns participants to a tested intervention. The registered 128 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).

The record links to 0 conditions, and to 2 interventions - of which Strategy Training is the first listed.

NCT01934621 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01934621 about?

NCT01934621 is a clinical study titled "Adapting Daily Activity Performance Through Strategy Training". Individuals with cognitive impairments after stroke sustain significant disability in their daily tasks, and account for a significant proportion of stroke-related healthcare costs. The proposed study examines a novel intervention, strategy training, that shows promise for helping individuals with s...

What is the current status of trial NCT01934621?

This trial is currently completed. It is a NA study. The enrollment target is 128 participants. The study started on 2013-11. Estimated completion is 2020-09.

What interventions are being tested in trial NCT01934621?

The interventions under investigation include: Strategy Training (BEHAVIORAL), Attention Control (BEHAVIORAL).

Who is sponsoring clinical trial NCT01934621?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01934621's enrollment target sits among peer trials

128 744th of 2000 higher than 1,252 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

  • NCT02870738 · 128 participants · Phase 2

    Bladder Directed vs. Pelvic Floor Therapy in IC/BPS

  • NCT03294460 · 128 participants · Phase 1

    Nicotinic Receptor Genetic Variation and Alcohol Reward

  • NCT04149977 · 128 participants · NA

    Blood Flow Restriction Therapy in Lower Limb Extensor Injuries

  • NCT04373057 · 128 participants · Phase 1

    Prebiotic Galacto-oligosaccharide and Acute GVHD

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 NCT01934621, the US trial registry maintained by the National Library of Medicine. NCT01934621 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.