Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Head and Neck Cancer
Type
Interventional
Phase
Not Applicable
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Supportive Care

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

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. H1...

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

Tracking Information

NCT #
NCT04830488
Collaborators
Not Provided
Investigators
Principal Investigator: Bethany Rhoten, PhD Vanderbilt Medical Center