Comparison between in-person and couples counseling in reducing anxiety depression and quality of life of HPV positive women

Comparison of in-person and couples counseling on anxiety, depression and quality of life in HPV-positive women

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20201012049002N1

Enrollment

120

Registered

2021-01-09

Start date

2021-01-14

Completion date

Unknown

Last updated

2021-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Anogenital (venereal) warts. Condition 2: Mild cervical dysplasia. Anogenital (venereal) warts Mild cervical dysplasia

Interventions

Intervention 1: Intervention group 1: This intervention will run virtually and individually in 6 sessions (30 minutes for each session) as a day in between. Telephone counseling to support women with

Eligibility

Sex/Gender

All

Age

18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Receiving Positive result of HPV test Being literate Understanding Persian language no chronic illness no known mental illness

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Anxiety and Depression. Timepoint: Before the intervention and 8 weeks after the intervention. Method of measurement: Hospital Anxiety and Depression Scale (HADS).	—

Secondary

Measure	Time frame
Quality of life. Timepoint: Before and 10 weeks after intervention. Method of measurement: QoL SF-36.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyedeh Tahereh Mirmolaei

Tehran University of Medical Sciences

mirmolaei@tums.ac.ir+98 21 6105 4000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026