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NCT05305235 · ClinicalTrials.gov registry record · NA

RCT for Innovating Stress-related eHealth

A NA study, sponsored by University of North Carolina, Chapel Hill.

Completed
Registry status
NA
Development phase
75
Enrollment target

NCT05305235: Completed NA study, sponsored by University of North Carolina, Chapel Hill.

NCT05305235 is a NA study that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 75 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05305235, a NA study, has completed, sponsored by University of North Carolina, Chapel Hill.

COMPLETED
Registry status
NA
Development phase
75 participants
Enrollment target

Study Summary

The Randomized Control Trial for Innovating Stress-related eHealth (RISE) Study tests the hypotheses that a highly promising digital therapeutic (RISE Guide) targeting anxiety sensitivity (AS) will be acceptable to women sexual assault survivors; reduce survivors' anxiety sensitivity, and, in turn, posttraumatic stress. If successful, RISE Guide could be provided at no cost to all women who present to US emergency departments for emergency care after sexual assault.

Primary Outcome

The Treatment Adherence/Acceptability Scale (TAAS) is a 10-item measure of treatment acceptability (e.g., I would recommend this treatment to a friend) and adherence (e.g., I would be able to finish \[this treatment\]) that participants rate on a 7-point Likert scale with scores ranging from 10-70. Higher scores indicate higher acceptability.

Interventions

  • DEVICE RISE Guide
  • DEVICE Relaxation Control

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2021-12-01
Est. Completion 2024-02-24
Phase NA

What the finished NCT05305235 record still lists

NCT05305235 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 75 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

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

NCT05305235 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05305235 about?

NCT05305235 is a clinical study titled "RCT for Innovating Stress-related eHealth". The Randomized Control Trial for Innovating Stress-related eHealth (RISE) Study tests the hypotheses that a highly promising digital therapeutic (RISE Guide) targeting anxiety sensitivity (AS) will be acceptable to women sexual assault survivors; reduce survivors' anxiety sensitivity, and, in turn, ...

What is the current status of trial NCT05305235?

This trial is currently completed. It is a NA study. The enrollment target is 75 participants. The study started on 2021-12-01. Estimated completion is 2024-02-24.

What interventions are being tested in trial NCT05305235?

The interventions under investigation include: RISE Guide (DEVICE), Relaxation Control (DEVICE).

Who is sponsoring clinical trial NCT05305235?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05305235's enrollment target sits among peer trials

75 1069th of 2000 higher than 919 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

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Source: ClinicalTrials.gov NCT05305235, the US trial registry maintained by the National Library of Medicine. NCT05305235 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.