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New phone programs ease cancer survivors' symptoms and distress

NCT ID NCT05360498

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

Summary

This study tested two phone-based programs for cancer survivors and their caregivers to help manage physical and emotional symptoms after treatment ends. 555 survivors and their caregivers took part. The programs provided information and counseling to reduce distress and improve well-being, especially for those in rural areas with limited access to care.

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

555 people

The number who actually took part.

Started

Aug 2022

Finished

Jan 2026

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

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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 for the survivors: 1. age 18 or older 2. within 4 weeks of completing or within 2 years of having completed cancer treatment with curative intent 3. able to perform basic activities of daily living 4. cognitively oriented to time, place, and person (recruiter determined) 5. able to speak and understand English or Spanish 6. access to a telephone 7. has a caregiver who can be any relationship role (e.g., spouse, sibling, parent, friend) who can participate with them. Inclusion criteria for the caregivers: 1. age 18 or older 2. able to speak and understand English or Spanish 3. telephone access 4. not currently receiving counseling and/or psychotherapy 5. not currently treated for cancer Exclusion criteria for the survivors: 1. Less than 18 years of age 2. Diagnosis of psychotic disorder 3. Nursing home resident 4. Bedridden 5. Currently receiving counseling and/or psychotherapy Exclusion criteria for caregiver: 1. Less than 18 years of age 2. Currently treated for cancer to preserve the distinguishability of "survivor" and "caregiver" 3. Currently receiving counseling and/or psychotherapy

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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.

Contacts and locations

Locations

  • University of Arizona

    Tucson, Arizona, 85724, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.