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Body Image After Head and Neck Cancer Treatment (BIHNC)

B

Bethany Rhoten

Status

Completed

Conditions

Head and Neck Cancer

Treatments

Behavioral: e-learning didactic module
Behavioral: Personal reflection activities

Study type

Interventional

Funder types

Other

Identifiers

NCT04830488
VICC HN 2123

Details and patient eligibility

About

This is a pilot study of the Body Image after Head and Neck Cancer Treatment Program [BIHNC]. It is a six-week, psychoeducational, web-based program that includes e-learning didactic modules and personal reflection activities for participants to complete.

Full description

Specific Aim 1: To assess the feasibility and acceptability of [BIHNC] in patients who have completed treatment for head and neck cancer and who have body image concerns.

H1a: Eighty percent of enrolled study participants who complete baseline self-report measures will complete the BIHNC Program.

H1b: Eighty percent of study participants completing the BIHNC Program will rate it acceptable on the intervention evaluation form.

Specific Aim 2: To assess the preliminary efficacy of BIHNC for reducing body image concerns in patients who have completed treatment for head and neck cancer and who have body image concerns.

H2: Body image scores will improve from pre- to post- intervention

Enrollment

7 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Completion of any form of head and neck cancer treatment between 3 and 24 months previously at study enrollment
  • Answer in the affirmative to at least one of two questions concerning dissatisfaction with the way their body looks or function
  • Have clinically significant body image concerns as defined by (BIS score > 10)

Exclusion criteria

  • Undergoing head and neck cancer treatment at time of study enrollment
  • Cognitive impairment that would preclude ability to provide informed consent
  • Unable to read text on a computer screen
  • Not able to read and understand English

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

7 participants in 1 patient group

Body Image after Head and Neck Cancer Treatment
Experimental group
Treatment:
Behavioral: Personal reflection activities
Behavioral: e-learning didactic module

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Vanderbilt-Ingram Service Information Program; Bethany Rhoten, PhD

Data sourced from clinicaltrials.gov

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