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

NCT03681405 · ClinicalTrials.gov registry record · NA

Supportive Programs for Supporting Optimal Recovery in Participants Undergoing Gynecological Surgery

A NA study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
NA
Development phase
31
Enrollment target

NCT03681405: Completed NA study, sponsored by Wake Forest University Health Sciences.

NCT03681405 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 31 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03681405, a NA study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
NA
Development phase
31 participants
Enrollment target

Study Summary

This trial studies how well two different supportive programs work in supporting optimal recovery in participants undergoing gynecological surgery. Supportive programs use different methods for helping participants cope with the surgical experience including gentle movements, counseling, writing, or relaxation techniques, and may help improve participants' well-being after gynecological surgery.

Primary Outcome

Will provide quantitative data to guide future study planning. Will calculate 95% confidence intervals for each of the feasibility measures to determine the range of estimates that are consistent with the data. Will track the number of screened participants, those who are eligible, and the percent who agree to participate. For those not meeting the eligibility criteria, reasons will be summarized. The proportion of participants and corresponding 95% CI for participants who participated in each g

Interventions

  • OTHER Questionnaire Administration
  • OTHER Informational Intervention
  • BEHAVIORAL Telephone-Based Intervention

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2018-12-07
Est. Completion 2020-04-09
Phase NA
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT03681405 record still lists

NCT03681405 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 3 interventions - of which Questionnaire Administration is the first listed.

NCT03681405 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03681405 about?

NCT03681405 is a clinical study titled "Supportive Programs for Supporting Optimal Recovery in Participants Undergoing Gynecological Surgery". This trial studies how well two different supportive programs work in supporting optimal recovery in participants undergoing gynecological surgery. Supportive programs use different methods for helping participants cope with the surgical experience including gentle movements, counseling, writing, or...

What is the current status of trial NCT03681405?

This trial is currently completed. It is a NA study. The enrollment target is 31 participants. The study started on 2018-12-07. Estimated completion is 2020-04-09.

What interventions are being tested in trial NCT03681405?

The interventions under investigation include: Questionnaire Administration (OTHER), Informational Intervention (OTHER), Telephone-Based Intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT03681405?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03681405's enrollment target sits among peer trials

31 1592nd of 2000 higher than 408 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

  • NCT02932618 · 31 participants · Phase 3

    A Study of Recombinant Von Willebrand Factor (rVWF) With or Without ADVATE in Children With Severe Von Willebrand Disease (VWD)

  • NCT03482297 · 31 participants · Phase 1

    Automated Abdominal Binder for Orthostatic Hypotension

  • NCT04016389 · 31 participants · NA

    FIGO 2018 Stage IB2 Cervical Cancer Treated With Neoadjuvant Chemotherapy Followed by Fertility Sparing Surgery

  • NCT04211675 · 31 participants · Phase 1

    NK Cells Infusions With Irinotecan, Temozolomide, and Dinutuximab

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03681405, the US trial registry maintained by the National Library of Medicine. NCT03681405 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.