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NCT02492100 · ClinicalTrials.gov registry record · NA

A Multimodal Intervention to Address Sexual Dysfunction in Hematopoietic Stem Cell Transplant Survivors

A NA study, sponsored by Massachusetts General Hospital.

Completed
Registry status
NA
Development phase
47
Enrollment target

NCT02492100: Completed NA study, sponsored by Massachusetts General Hospital.

NCT02492100 is a NA study that has completed, run by Massachusetts General Hospital. The registered enrollment target is 47 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 ↗

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The verdict

NCT02492100, a NA study, has completed, sponsored by Massachusetts General Hospital.

COMPLETED
Registry status
NA
Development phase
47 participants
Enrollment target

Study Summary

This research study is evaluating the feasibility and impact of an intervention to improve sexual function in stem cell transplant survivors on participants' sexual function, quality of life, and mood. \- It is expected that about 50 stem cell transplant survivors will take part in this research study.

Primary Outcome

intervention deemed feasible if at least 75% of patients screening positive for sexual dysfunction causing distress agree to participate and at least 80% complete at least one additional follow-up visit. This is not a composite outcome. Study is deemed feasible (yes) if both criteria are met.

Interventions

  • BEHAVIORAL Multi-modality sexual dysfunction intervention

Trial Details

FieldValue
Enrollment Target 47 participants
Start Date 2015-06
Est. Completion 2017-12
Phase NA
Massachusetts General Hospital

2,032 total trials

What the finished NCT02492100 record still lists

NCT02492100 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 47 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 1 intervention - of which Multi-modality sexual dysfunction intervention is the first listed.

NCT02492100 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02492100 about?

NCT02492100 is a clinical study titled "A Multimodal Intervention to Address Sexual Dysfunction in Hematopoietic Stem Cell Transplant Survivors". This research study is evaluating the feasibility and impact of an intervention to improve sexual function in stem cell transplant survivors on participants' sexual function, quality of life, and mood. \- It is expected that about 50 stem cell transplant survivors will take part in this research st...

What is the current status of trial NCT02492100?

This trial is currently completed. It is a NA study. The enrollment target is 47 participants. The study started on 2015-06. Estimated completion is 2017-12.

What interventions are being tested in trial NCT02492100?

The interventions under investigation include: Multi-modality sexual dysfunction intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT02492100?

This trial is sponsored by Massachusetts General Hospital, which has 2,032 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02492100's enrollment target sits among peer trials

47 1400th of 2000 higher than 599 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 NCT02492100, the US trial registry maintained by the National Library of Medicine. NCT02492100 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.