Parenting Support Intervention for Families Coping With Metastatic or Locally Recurrent Solid Tumor Diagnosis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorM.D. Anderson Cancer Center

About this trial

This clinical trial examines the acceptability and effect of a parenting support intervention for families coping with solid tumor that has spread to other places in the body (metastatic) or has come back (recurrent). Parenting support program may help to reduce common parenting concerns, improve communication between parents and children about cancer, and improve the overall psychological wellbeing of parents.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Participants must (1) be diagnosed with a metastatic or locally recurrent solid malignant tumor and on active treatment; (2) be at least 18 years old; (3) have at least one dependent child between the ages of 4 and 17 and currently living with the parent; (4) be able to provide informed consent and (5) have a spousal caregiver over the age of 18 who co-parents the child(ren) (i.e. share custody) and is willing and able to consent to participate.*

Disqualifiers

Participants and caregivers who do not read and speak English and who do not have access to the internet.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Best Practice

    Other intervention

    Receive standard of care

  • Educational Intervention

    Other intervention

    Receive educational materials and attend videoconference sessions

  • Questionnaire Administration

    Other intervention

    Ancillary studies

Treatment groups

120 Participants
are divided into 2 treatment groups
Group A: Group I (education material, videoconference session)Experimental treatment 2 interventions
Group B: Group II (waitlist control)Active comparator 2 interventions

Trial outcomes

Primary outcomes

1

Examine the feasibility of implementing a parenting support intervention in 50 patients with an incurable cancer and their spousal caregivers.

Time frame
Through study completion, an average of 1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

M.D. Anderson Cancer Center

Lead sponsor

National Cancer Institute (NCI)

Collaborator