Peer Support Program for Improving Quality of Life Among Head and Neck Patients, Connecting Through Cancer Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-89
SponsorOHSU Knight Cancer Institute

About this trial

This clinical trial tests whether a peer support program is feasible for head and neck cancer patients. Social support at the time of diagnosis has been shown to improve head and neck cancer quality of life before and after treatment. However, not all patients have a strong social support system. Recent research has shown that peer support programs have the potential to address unmet social support needs among cancer patients. These programs involve cancer survivors (peer mentors) providing emotional and informational support to cancer patients (mentees) earlier in their disease course. Peer support programs may also reduce caregiver burden by providing an additional source of support for the patient. A one-on-one peer support program may be feasible for patients with head and neck cancer and their caregivers.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

MENTEE GROUP: Ability to understand and the willingness to sign a written informed consent document

MENTEE GROUP: Willingness to have mentor-mentee interactions with the mentor selected by Imerman Angels (documented as part of informed consent)

MENTEE GROUP: Age 18 or older at the time of consent (upper age limit 89)

MENTEE GROUP: Diagnosed with head & neck cancer (all stages) and planning to receive, currently receiving or recently completed (within 12 months) active treatment OR in follow-up and reporting unmet social/support needs

Disqualifiers

MENTEE GROUP: Mentee must not be regularly engaging in other support programs at the start of the study intervention

MENTEE GROUP: Undergoing active professional treatment for cognitive or emotional difficulties or neurological deficits that preclude adherence to the study protocol

MENTEE GROUP: Any other social, emotional, or personal situation that will preclude adherence to the study protocol, at the discretion of the investigator

CAREGIVER GROUP: Caregivers must not be regularly engaging in other support programs at the start of the study intervention

Trial design

Design model

Single group

Treatments tested in this trial

  • Supportive Care

    Other intervention

    Participate in peer support program

  • Survey Administration

    Other intervention

    Ancillary studies

  • Interview

    Other intervention

    Ancillary studies

Treatment groups

56 Participants
are divided into 1 treatment group
Group A: Supportive Care (peer support program)Experimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

Proportion of mentees meeting with their mentor match at least once

Will be reported with 95% asymptotic confidence interval.

Time frame
Up to 6 months

Secondary outcomes

1

Satisfaction with peer mentor contacts

Satisfaction will be measured using a survey that was used in a prior pilot study on a one-on-one cancer peer support program by Valanjow and Weis (2024). The survey contains 14 statements and mentees will be asked to rate how much they feel the statement applies. The scale ranges from 1-5 (1= not applicable and 5=fully applies). Mean and standard deviation of the Likert score will be reported for each item at each time point.

Time frame
Up to 6 months
2

Utilization of the mentorship program

Mean and standard deviation will be reported for number of times the mentor and mentee have made contact.

Time frame
Up to 6 months
3

Mentorship conversation topics

Proportions of categories will be reported for topics discussed between mentor and mentee.

Time frame
Up to 6 months
4

Rating scale for match

Mean and standard deviation will be reported for rating scale for match (in terms of similar demographics and cancer experience). This will be on a 1-10 scale, with 10 being the most similar match.

Time frame
Up to 6 months

Other outcomes

1

Mentee psychosocial well-being over time

Mentees will complete short surveys analyzing coping, anxiety and depression at three different time points to track changes over time.

Time frame
Up to 6 months
2

Caregiver burden over time (optional)

Caregivers will complete surveys on caregiver burden at three different time points to track changes over time.

Time frame
Up to 6 months

Sponsors and contacts

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OHSU Knight Cancer Institute

Lead sponsor

Oregon Health and Science University

Collaborator

This trial is not recruiting at the moment. You can still explore other options: