CClinicalTrials.gg
CompletedNCT05087004Updated Oct 21, 2021

Planned Parenthood Teen Council Program Study

An interventional study of Teen Council in Adolescent Problem Behavior, sponsored by Philliber Research & Evaluation. Completed. Open to participants aged 14 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-10-21.

Sponsored by Philliber Research & Evaluation · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 7 years 3 months after the study started (first participant enrolled Jun 2014, registered Sep 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
810
Allocation
Randomized
Ages
14 Years to 18 Years
Sex
All
01

Study summary

This is a randomized controlled trial (RCT) evaluation of the Teen Council program that was tested with high school students (grades 10-12) to assess whether it results in a reduction of teen pregnancy among other outcomes.

Read the detailed description

Over the course of five years, we expected to have approximately 800 teens (400 program and 400 control) in the study. Teens were randomly selected for the program (Teen Council) and control (no program) conditions.

Teens in both groups were surveyed in the late summer/early fall of their enrollment year and each spring thereafter. Participation in the evaluation by control teens and unenrolled program teens was recognized with a small stipend.

The pre-survey was administered during the summer retreat for incoming Teen Council members. The same survey was administered by Philliber staff for the control youth via online, telephone, or mailed surveys during the late summer/fall. The post-surveys were administered at the end of the school year. Again, the survey was administered by program facilitators for the Teen Council program group. Philliber administered the post survey for the control group providing the same options for completion (online, telephone, or mail).

To facilitate follow-up, complete contact information was collected at baseline. This included the telephone numbers, physical addresses, and email addresses of the student and telephone numbers of their parents/guardians. Also requested was contact information for two relatives or adult friends who would likely know how to contact the teen. Parents were asked on the consent form to provide permission to receive change of school information in the event that their teen transferred to a new school. Philliber reached out to unenrolled Teen Council members and control group teens by telephone, email, text messaging, and/or U.S. Mail for survey administration (via telephone, online, or hard copy).

02

Conditions studied

  • Adolescent Problem Behavior

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Keywords

  • Adolescent pregnancy prevention
  • Youth development
03

In context

Problem Behavior

517 studies on the registry are indexed under Problem Behavior; 92 are open to participants now.

This study's enrollment of 810 is above the median of 90 across 391 interventional studies indexed under Problem Behavior.

Browse Problem Behavior studies →

Lead sponsor

Philliber Research & Evaluation is the lead sponsor of 8 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
14 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

Applicants had to be:

  1. entering 10th, 11th, or 12th grades;
  2. able to attend an annual mandatory overnight retreat;
  3. interested in providing accurate sexual health information to peers;
  4. able to commit to weekly meetings;
  5. able to miss school occasionally for presentations (one day per month);
  6. responsible for budgeting their time and keeping up with their academic work.

Exclusion criteria

Exclusion Criteria:

Any interested participant who did not meet all of the inclusion criteria:

  1. was not entering 10th, 11th, or 12th grades;
  2. was not able to attend an annual mandatory overnight retreat;
  3. was not interested in providing accurate sexual health information to peers;
  4. was not able to commit to weekly meetings;
  5. was not able to miss school occasionally for presentations (one day per month); (6) was not responsible for budgeting their time and keeping up with their academic work.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
810 participants (actual)

Study arms

  • Experimental
    Teen Council Pogram

    Teens assigned to the intervention group received a 1-year long Teen Council Program.

    Behavioral: Teen Council

  • No intervention
    Control Group

    Teens assigned to the control group did not receive any intervention.

Interventions

  • BehavioralTeen Council

    Youth randomly selected for Teen Council attended weekly meetings for an entire school year to receive training on specific topics. In turn, they provided educational presentations to the community, which required that they miss school (about one day per month). The presentations Teen Council members offered in middle and high schools were most commonly on birth control methods; relationships; reproductive anatomy and physiology; sexual diversity; STDs/STIs; sexual consent; HIV/AIDS; and abstinence.

06

What researchers measure

Primary outcomes

  1. Ever had sex

    Study participants were asked, "Have you ever had sexual intercourse?" Sexual intercourse was defined as any oral, anal, or penis-in-vagina sex. Item response choices were Yes/No.

    Time frame: Prior to program participation (baseline)

  2. Ever had sex

    Study participants were asked, "Have you ever had sexual intercourse?" Sexual intercourse was defined as any oral, anal, or penis-in-vagina sex. Item response choices were Yes/No.

    Time frame: 1 year

  3. Contraceptive use at last intercourse

    Study participants were asked, "The last time you had sexual intercourse, which methods did you or your partner use to prevent pregnancy?" Item response options included: I have never had penis-in-vagina sexual intercourse; no method was used to prevent pregnancy; birth control pills; condoms; Depo-Provera (or any injectable birth control), Nuva Ring (or any birth control ring), Implanon (or any implant), birth control patch, or any IUD; withdrawal; some other method; and not sure. These responses were recoded to Yes/No.

    Time frame: Prior to program participation (baseline)

  4. Contraceptive use at last intercourse

    Study participants were asked, "The last time you had sexual intercourse, which methods did you or your partner use to prevent pregnancy?" Item response options included: I have never had penis-in-vagina sexual intercourse; no method was used to prevent pregnancy; birth control pills; condoms; Depo-Provera (or any injectable birth control), Nuva Ring (or any birth control ring), Implanon (or any implant), birth control patch, or any IUD; withdrawal; some other method; and not sure. These responses were recoded to Yes/No.

    Time frame: 1 year

  5. Changes to contraceptive method in last year

    Study participants were asked, "During the last year, have you made any changes in the use of protection from sexually-transmitted infections (STIs) or pregnancy? Item response categories included: I have never had sexual intercourse; I haven't had sexual intercourse in the past 12 months; no; yes. If response was yes, study participants were asked to identify their previous contraceptive method and their current contraceptive method. Contraceptive methods were coded as reliable or not reliable.

    Time frame: Prior to program participation (baseline)

  6. Changes to contraceptive method in last year

    Study participants were asked, "During the last year, have you made any changes in the use of protection from sexually-transmitted infections (STIs) or pregnancy? Item response categories included: I have never had sexual intercourse; I haven't had sexual intercourse in the past 12 months; no; yes. If response was yes, study participants were asked to identify their previous contraceptive method and their current contraceptive method. Contraceptive methods were coded as reliable or not reliable.

    Time frame: 1 year

  7. Ever visited doctor/clinic for birth control, exam, or STI

    Study participants were asked, "j. Have you ever been to a doctor or to a clinic to get birth control, to have a pelvic exam, a testicular exam or to get a check up for sexually transmitted infections?" Item responses were Yes/No.

    Time frame: Prior to program participation (baseline)

  8. Ever visited doctor/clinic for birth control, exam, or STI

    Study participants were asked, "j. Have you ever been to a doctor or to a clinic to get birth control, to have a pelvic exam, a testicular exam or to get a check up for sexually transmitted infections?" Item responses were Yes/No.

    Time frame: 1 year

Secondary outcomes

  1. Comfort with own sexuality scale

    Seven-items that measured such things as comfort talking with a date about sex or birth control and having a good understanding of one's own sexual feelings and reactions (alpha = 0.7545). Each item was rated on a scale of 1 to 4, with the most desirable response being 4.

    Time frame: Prior to program participation (baseline)

  2. Comfort with own sexuality scale

    Seven-items that measured such things as comfort talking with a date about sex or birth control and having a good understanding of one's own sexual feelings and reactions (alpha = 0.7545). Each item was rated on a scale of 1 to 4, with the most desirable response being 4.

    Time frame: 1 year

  3. Confidence in peer education skills scale

    Eight-items, on a scale of 1 to 4, that measured confidence in accessing current information about sexually transmitted diseases and infections or explaining proper condom usage to peers (alpha = 0.7525).

    Time frame: Prior to program participation (baseline)

  4. Confidence in peer education skills scale

    Eight-items, on a scale of 1 to 4, that measured confidence in accessing current information about sexually transmitted diseases and infections or explaining proper condom usage to peers (alpha = 0.7525).

    Time frame: 1 year

  5. Civic action scale

    Six-item scale adapted from Flanagan et al. to measure ability to be actively engaged citizens (alpha = 0.6789). The scale, rated on a scale of 1 to 4, measured such things as the strength of their belief that they can make a difference in their communities and confidence that they can express their views in front of a group.

    Time frame: Prior to program participation (baseline)

  6. Civic action scale

    Six-item scale adapted from Flanagan et al. to measure ability to be actively engaged citizens (alpha = 0.6789). The scale, rated on a scale of 1 to 4, measured such things as the strength of their belief that they can make a difference in their communities and confidence that they can express their views in front of a group.

    Time frame: 1 year

  7. Perspective taking scale

    Seven-item sub-scale from the Interpersonal Reactivity Index measuring the ability of youth to be empathetic and understand the perspective of others (alpha = 0.7158). This 5-point subscale included items to measure attempts to understand their friends by imagining how things look from their perspective and trying to look at both sides of every question. The scale language was adapted to be more gender neutral, with permission of the author.

    Time frame: Prior to program participation (baseline)

  8. Perspective taking scale

    Seven-item sub-scale from the Interpersonal Reactivity Index measuring the ability of youth to be empathetic and understand the perspective of others (alpha = 0.7158). This 5-point subscale included items to measure attempts to understand their friends by imagining how things look from their perspective and trying to look at both sides of every question. The scale language was adapted to be more gender neutral, with permission of the author.

    Time frame: 1 year

  9. Communication with parents

    Two items about teen comfort talking with parents about sex and birth control, rated 1 to 4, with 4 indicating the highest level of comfort. These two items were examined individually. A third item measured whether youth had conversations with parents about sexuality or birth control in the past year (yes/no). A final item had teens report the number of such conversations in five unequal categories (0,1-5, 6-10, 11-15, and more than 15), then dichotomized to 10 or fewer conversations (0) and more than ten conversations (1).

    Time frame: Prior to program participation (baseline)

  10. Communication with parents

    Two items about teen comfort talking with parents about sex and birth control, rated 1 to 4, with 4 indicating the highest level of comfort. These two items were examined individually. A third item measured whether youth had conversations with parents about sexuality or birth control in the past year (yes/no). A final item had teens report the number of such conversations in five unequal categories (0,1-5, 6-10, 11-15, and more than 15), then dichotomized to 10 or fewer conversations (0) and more than ten conversations (1).

    Time frame: 1 year

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No — Full study report is available upon request.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 21, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05087004
Lead sponsor
Philliber Research & Evaluation
Responsible party
Sally Brown (Senior Researh Associate, Philliber Research & Evaluation) — Principal investigator
First posted
Oct 21, 2021
Start date
Jun 1, 2014
Primary completion
Aug 6, 2019
Completion
Aug 6, 2019
Last update
Oct 21, 2021

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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