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

NCT02663778 · ClinicalTrials.gov registry record · NA

Task Specific Timing and Coordination Exercise to Improve Mobility in Older Adults: Program to Improve Mobility in Aging

A NA study of Gait, Unsteady, sponsored by University of Pittsburgh.

Completed
Registry status
NA
Development phase
353
Enrollment target
1
Study location

NCT02663778: Completed NA study of Gait, Unsteady, sponsored by University of Pittsburgh.

NCT02663778 is a NA study of Gait, Unsteady that has completed, run by University of Pittsburgh. The registered enrollment target is 353 participants, above the 51-participant average among 3 other Gait, Unsteady trials with a reported enrollment target (592% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02663778, a NA study of Gait, Unsteady, has completed, sponsored by University of Pittsburgh.

COMPLETED
Registry status
NA
Development phase
353 participants
Enrollment target
1
Study location

Study Summary

This randomized clinical trial targets 248 community-dwelling older adults with impaired mobility (i.e. walking slowly; gait speed \< 1.20 m/s). The trial compares a 12 week "standard-plus" program of strength, endurance, flexibility plus task specific timing and coordination training to a standard 12 week strength, endurance and flexibility program. The primary outcome is gait speed at 12 weeks. Secondary and tertiary outcomes represent components of the intervention and measures of activity and participation. Delayed and sustained effects of the intervention are examined at 24 and 36 weeks.

Primary Outcome

Usual walking speed over a short distance. A physiologic measure recorded in m/s.

Conditions Studied

Interventions

  • BEHAVIORAL Strength training
  • BEHAVIORAL Endurance training
  • BEHAVIORAL Flexibility training
  • BEHAVIORAL Task Specific timing and coordination training
  • BEHAVIORAL Physical activity behavioral intervention

Study Locations (1)

Pennsylvania

  • University of Pittsburgh - Pittsburgh

Trial Details

FieldValue
Enrollment Target 353 participants
Start Date 2016-04
Est. Completion 2021-02
Phase NA
University of Pittsburgh

1,238 total trials

What the finished NCT02663778 record still lists

NCT02663778 is an interventional study that assigns participants to a tested intervention. The registered 353 participants enrollment target is mid-sized for trials with a published cap, above the 51-participant average among 3 other Gait, Unsteady trials with a reported enrollment target (592% higher).

The record links to 1 condition, with Gait, Unsteady appearing as the primary indexed condition, and to 5 interventions - of which Strength training is the first listed.

NCT02663778 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT02663778 about?

NCT02663778 is a clinical study titled "Task Specific Timing and Coordination Exercise to Improve Mobility in Older Adults: Program to Improve Mobility in Aging". This randomized clinical trial targets 248 community-dwelling older adults with impaired mobility (i.e. walking slowly; gait speed \< 1.20 m/s). The trial compares a 12 week "standard-plus" program of strength, endurance, flexibility plus task specific timing and coordination training to a standard ...

What is the current status of trial NCT02663778?

This trial is currently completed. It is a NA study. The enrollment target is 353 participants. The study started on 2016-04. Estimated completion is 2021-02.

What conditions does trial NCT02663778 study?

This clinical trial studies the following conditions: Gait, Unsteady.

What interventions are being tested in trial NCT02663778?

The interventions under investigation include: Strength training (BEHAVIORAL), Endurance training (BEHAVIORAL), Flexibility training (BEHAVIORAL), Task Specific timing and coordination training (BEHAVIORAL), Physical activity behavioral intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT02663778?

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

Where is trial NCT02663778 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Gait, Unsteady

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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

  • NCT05548296 · 353 participants · Phase 2

    A Phase 2 Study of ACR-368 in Endometrial Adenocarcinoma

  • NCT05884775 · 353 participants · NA

    Novel Digital Patient-Reported Outcomes Tool for Diabetes Management

  • NCT02579967 · 354 participants · Phase 2

    Pilot Trial of Allogeneic Blood or Marrow Transplantation for Primary Immunodeficiencies

  • NCT02610413 · 354 participants

    Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Hypertension Receiving Bevacizumab for Breast Cancer

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 NCT02663778, the US trial registry maintained by the National Library of Medicine. NCT02663778 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.