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

NCT07221071 · ClinicalTrials.gov registry record · NA

Supporting Women With Breast Cancer to Prepare for Treatment (The Prepare Study)

A NA study, sponsored by Endeavor Health.

Completed
Registry status
NA
Development phase
42
Enrollment target

NCT07221071: Completed NA study, sponsored by Endeavor Health.

NCT07221071 is a NA study that has completed, run by Endeavor Health. The registered enrollment target is 42 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07221071, a NA study, has completed, sponsored by Endeavor Health.

COMPLETED
Registry status
NA
Development phase
42 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate if a brief mindfulness intervention before and after surgery would impact patient emotional wellbeing, quality of life, and biomarkers measured before and after surgery by finger prick collection and surveys.

Primary Outcome

To measure the impact of a mindfulness intervention instituted prior to surgery on patient anxiety for newly diagnosed breast cancer patients, using the PROMIS anxiety questionnaire \[Emotional Distress - Anxiety - Short Form 8a answer options are: Never, Rarely, Sometimes, Often, Always\].

Interventions

  • BEHAVIORAL Mindfulness Arm
  • OTHER Control group placebo

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2021-08-05
Est. Completion 2024-12-31
Phase NA
Endeavor Health

94 total trials

What the finished NCT07221071 record still lists

NCT07221071 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

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

NCT07221071 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07221071 about?

NCT07221071 is a clinical study titled "Supporting Women With Breast Cancer to Prepare for Treatment (The Prepare Study)". The purpose of this study is to evaluate if a brief mindfulness intervention before and after surgery would impact patient emotional wellbeing, quality of life, and biomarkers measured before and after surgery by finger prick collection and surveys.

What is the current status of trial NCT07221071?

This trial is currently completed. It is a NA study. The enrollment target is 42 participants. The study started on 2021-08-05. Estimated completion is 2024-12-31.

What interventions are being tested in trial NCT07221071?

The interventions under investigation include: Mindfulness Arm (BEHAVIORAL), Control group placebo (OTHER).

Who is sponsoring clinical trial NCT07221071?

This trial is sponsored by Endeavor Health, which has 94 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07221071's enrollment target sits among peer trials

42 1436th of 2000 higher than 555 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

  • NCT02852213 · 42 participants · Phase 1

    A Single-Stage, Adaptive, Open-label, Dose Escalation Safety and Efficacy Study of AADC Deficiency in Pediatric Patients

  • NCT03136146 · 42 participants · Phase 2

    Combination Chemotherapy in Treating Patients With Relapsed or Refractory Acute Lymphoblastic Leukemia, Lymphoblastic Lymphoma, Burkitt Lymphoma/Leukemia, or Double-Hit Lymphoma/Leukemia

  • NCT03178149 · 42 participants · Phase 1

    A Study of the Safety and Tolerability of ASP7317 in Senior Adults Who Are Losing Their Clear, Sharp Central Vision Due to Geographic Atrophy Secondary to Dry Age-related Macular Degeneration

  • NCT03663530 · 42 participants · NA

    Circadian Misalignment and Energy Balance

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 NCT07221071, the US trial registry maintained by the National Library of Medicine. NCT07221071 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.