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Biofeedback training aims to restore sexual health in cervical cancer survivors

NCT ID NCT07597083

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether special pelvic floor exercises, guided by a biofeedback device, can improve sexual function in women who had radiation for cervical cancer. Sixty survivors with sexual problems will be randomly assigned to either biofeedback-assisted training or standard pelvic floor exercises for 8 weeks. The goal is to see if the biofeedback approach leads to better sexual health and pelvic muscle function.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
biofeedback-assisted pelvic floor muscle training
What this could lead to
If it works, this could offer a non-drug way to improve sexual function and pelvic floor health in cervical cancer survivors after radiation.
What could go wrong
This is a small, early-stage trial with only 60 participants. The intervention is behavioral, so results may vary, and it may not work for everyone.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 60 people

The number the study aims to enrol. It can still change while the study runs.

Started

May 2026

Expected to finish

Mar 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

30 to 60 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Female participants aged 30-60 years. 2. Histologically confirmed diagnosis of cervical cancer (any stage at diagnosis) and completion of primary treatment. 3. Completion of pelvic radiotherapy (external beam radiotherapy and/or brachytherapy) ≥3 months prior to enrollment. 4. Presence of radiation-induced sexual dysfunction, defined as a Female Sexual Function Index (FSFI) score ≤26.55. 5. Self-reported sexual activity within the previous 6 months. 6. Medically stable with no current oncologic indication for active treatment, confirmed by treating oncologist. 7. Ability to understand study procedures and provide written informed consent. Exclusion Criteria: 1. Evidence of recurrent, persistent, or metastatic cervical cancer. 2. Participation in pelvic floor muscle training or biofeedback-based rehabilitation within the previous 6 months. 3. Presence of severe pelvic organ prolapse (stage III-IV). 4. Active pelvic infection, pelvic inflammatory disease, or untreated vaginal infection. 5. Ongoing significant vaginal bleeding of unknown or pathological origin. 6. Untreated or active urinary tract infection at the time of enrollment. 7. Neurological disorders affecting pelvic floor function (e.g., spinal cord injury, multiple sclerosis). 8. Severe psychiatric illness or uncontrolled mental health disorder affecting participation. 9. Cognitive impairment preventing understanding of instructions or adherence to protocol. 10. Current pregnancy or planning pregnancy during the study period. 11. Participation in another interventional clinical or rehabilitation trial within the last 3 months or during the study period.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The places running it

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  2. The official record

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Contacts and locations

Locations

  • Out patient clinic , faculty of Physical Therapy, Beni Sueif university

    RECRUITING

    Banī Suwayf, Egypt

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